Koninklijke Philips N.V. NY Registry Shares

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Welcome to the Royal Philips Third Quarter 2022 Resorts Conference Call on Monday, October 24th, 2022. During the call, hosted by Mr. Roy Jakobs, CEO, and Mr. Abhijit Bhattacharya, CFO, all participants will be in a listen-only mode. After the introduction, there will be an opportunity to ask questions. Please note that this call will be recorded and replay will be available on the Investor Relations website of Royal Philips. I will now hand the conference over to Mr. Leandro Mazzoni, Head of Investor Relations. Please go ahead, sir.

Hi, everyone. Welcome to the Philips Third Quarter 2022 Results Call. I'm here with our new CEO, Roy Jakobs, who took charge recently on October 15th and our CFO Abhijit Bhattacharya. Roy and Abhijit will take you through the third quarter results and our performance improvement actions. After that, there will be an opportunity for Q&A. The press release and Q3 slide deck were published at 7 a.m. CET on our investor relations website. We also published an updated deck and frequently asked questions on the Respironics recall this morning. The full transcript of this call will be made available on the website later today. Before we start, I want to draw your attention to our safe harbor statement on screen. With that, I'll hand over to Roy.

Thanks Leandro, and thanks everyone for joining us this morning. As this is my first earnings call as CEO of the company, I would want to welcome you. I look forward and commit to a transparent and constructive engagement with our investors, analysts, and other stakeholders about our ambition to create value for shareholders and all other stakeholders. Philips is a great company with a strong brand, leading innovation and portfolio, strong customer base, and talented employees. Operating in an attractive health tech market. Our strategy and solutions resonate with our customers. But we do face multiple challenges and have not lived up to their and your expectations in recent years. The current macroeconomic environment and external and internal supply chain disruptions presented further challenges and our disappointing Q3 and 2022 performance reflects this. We are taking actions to turn things around urgently and realize our potential as responsible leader in health technology solutions. We will be laser focused on this. My immediate priority is to improve execution. We will do that by first further strengthening our patient safety and quality management and continuing to address the Respironics recall and regulatory and legal processes connected to this. Urgently improving our supply chain operations so that we restore supply, deliver on our strong order book and deliver better results. And third, simplifying our organization and the way we work to drive clear accountability and improve productivity and agility. Moreover, we are taking immediate steps to reduce the costs involved in running the company. This includes the difficult but necessary decision to immediately reduce our workforce by around 4,000 roles globally, subject to consultation with relevant workers' councils and social partners. A decision we do not take lightly and which we will implement with respect towards impacted colleagues, but one that is needed to cope with our current challenges. We expect that we can recognize the expected associated costs and see the connected savings in the coming quarters. In addition, we will continue to review areas to further improve our supply operations, invest in quality and simplify the way of working and remove organizational complexity. This is expected to result in additional restructuring and associated costs in 2023. We will elaborate on progress on this. The 2023 plan and the detailed plans to further strengthen Philips operations and drive shareholder value creation at our fourth quarter and annual results publication in January 2023. Our strong order book shows the strength of our solutions and portfolio for customers and we're going to stop at nothing to regain our upward performance trajectory and drive sustainable value creation. Our continued focus on innovation and customer partnerships will further strengthen our businesses and results. For example, in third quarter, we signed a 10-year agreement with a large university hospital in Japan for the expansion of its EICU program. We expanded our leading ultrasound portfolio with the FDA's market clearance for our new ultrasound 5000 compact system. And in connected care, we continue to successfully expand into ambulatory care solutions as supported by newly published research on the Philips mobile cardiac outpatient telemetry. Before I give the floor to Abhijit, I would like to provide an update on the Respironics recall. I want to emphasize again that patient safety is our absolute number one priority. We know how important these sleep apnoea devices are to patients and how they improve their lives, and as such, I do apologize for any inconvenience caused. We continue with a comprehensive outreach to engage with patients, clinicians, and regulators. We know that patients are waiting. and we're doing everything we can to get the devices to them as soon as possible. We have significantly further increased our production capacity, reaching four times pre-recall levels. As of today, we have produced approximately 4 million devices and expect to produce and ship around 9% of the registered effect devices by end of 2022. Further biocompatibility testing and assessment of P per foam is ongoing to fully assess potential patient risk and to complement earlier released test data showing encouraging results. On the regulatory front, while we do understand that you would like to know more about the proposed consent decree, we are still in discussions with the DOJ and therefore cannot provide details related to the possible financial and operational impact at this time. In Q3, we recognized a non-cash charge for the impairment of goodwill of the sleep and respiratory care business. which Abhijit will further elucidate. Philips Respironics will continue to provide updates when and as appropriate. As Leandro mentioned, we have published FAQs and a presentation on the recall to provide details and clarification on the progress. There are some areas particularly related to litigation where we are not able to provide further details at this time. We will share information In open and timely manner as the situation evolves. I realize that I provide you with a lot of information in this first update from my side on results and on the issues to addressing quality, supply chain, and organization complexity. I do this so that you know what you can expect from Philips and from myself as CEO. With that, I would like to hand over to Abhijit.

Thank you, Roy, and good morning, everyone. Our performance in the third quarter was impacted by operational and supply challenges, inflationary pressures, the COVID situation in China and the Russia-Ukraine war. Comparable sales declined 5% in the quarter and adjusted EBITDA was 4.8% as pre-announced on October 12th. We have seen a gradual improvement in the supply chain situation and continue to take action to strengthen our supply chain resilience However, the progress has been slower than expected. We have been able to mitigate most of the supply chain issues in our personal health businesses. In the health systems businesses, it takes longer to see the impact of our actions given the regulated nature of the business and the installation-related risks from the customer side. All of this is expected to continue gradually ease in the coming years. It is important to note that these are not lost sales. The orders remain in our order book for future revenue recognition when we can fully deliver and install the equipment. Lower sales had an impact of 740 basis points in our adjusted EBITDA margin compared to the third quarter of 2021. Global inflation and cost headwinds also had significant impact Ph.D. Ph.D. Ph.D. Ph.D. regarding the estimated impact of the proposed consent decree and changes to the pre-tax discount rate. As disclosed, Philips Respironics is subject to an investigation by the U.S. Department of Justice, is a defendant in several class action lawsuits and individual personal injury claims, and is in ongoing discussions with the FDA regarding the consent decree. Given the uncertain nature and timing of the related events and of their potential impact and associated obligations, if any, the company has not made a provision in the accounts for these matters. Operating cash flow was an outflow of $180 million, mainly due to lower cash earnings, temporarily higher inventories, and cash costs related to the Respironics field actions. Let us now look at the performance per business. Diagnosis and treatment comparable sales declined 2% on the back of 10% growth in Q3 2021. Low single digit growth in image guided therapy was more than offset by a decline in ultrasound and diagnostic imaging due to specific electronic component shortages. Adjusted EBITDA margin was 9.1% The comparable sales for connected care declined 15% in the quarter, driven mainly by a substantial decline in the sleep and respiratory care business due to the recall, the operational challenges, and by supply chain headwinds in patient monitoring. Adjusted EBITDA amounted to a loss of 9.5% mainly due to the decline in sales and cost inflation. The personal health businesses' comparable sales grew by 4%, with high single-digit growth in oral health care and mother and child care and low single-digit growth in personal care. North America grew 7% while Western Europe grew double-digits. The adjusted EBITDA margin amounted to 14.1%. Now on orders, on the back of a strong 47% comparable order intake growth last year, order intake declined approximately 6% in the third quarter. The book-to-bill ratio remained strong at around 1.2% and the equipment order book grew further in the quarter. These order book metrics are depicted on page 15 of our investor relations deck. In our diagnosis and treatment business, orders were up 3% on the back of 15% increase in Q3 2021. Enterprise diagnostic informatics and image guided therapy orders grew high single digit. Diagnostic imaging grew mid single digit With another very strong quarter in magnetic resonance imaging. Connected care orders declined 24% in the quarter on the back of over 260% growth in Q3 last year. You will remember this was caused by the cancellation of the ventilator orders from the U.S. government. The average order growth over the last three years was 8% in connected care orders As we continue to experience good demand in the hospital patient monitoring business. Now I would like to update you on some of the key actions we are taking to step up performance. First on pricing. We have been raising pricing by mid single digit since the beginning of the year. In the personal health businesses, this is expected to have an impact of around 4% this year. In the diagnosis and treatment and connected care businesses, due to the longer equipment order book cycles, the impact of price increases will take longer to be fully realized in the profit and loss account. We expect around 1% impact this year and we will continue to take further pricing measures as needed. We said we are implementing productivity actions. Many of these initiatives have been communicated to you before but are being expanded or accelerated. In the supply chain, savings come from dual sourcing, supplier consolidation and the warehouse footprint rationalization. In quality, we are enhancing processes, increasing capabilities and product management. In R&D, we are shifting the focus to fewer High Impact Projects in the Innovation Pipeline. In connection with this action, we recorded a non-cash charge of €168 million in the third quarter, as reported earlier this month. Roy mentioned the difficult decision to immediately reduce our workforce by around 4,000 roles globally, which will have expected severance and termination-related costs of approximately 300 million in the coming quarters, of which about 150 million in the fourth quarter of this year. The associated cost savings are expected to amount to an annualized saving of 300 million. Very importantly, we continue to drive significant actions to increase supply chain resilience and mitigate the impact of disruptions. We are engaging with senior government officials, strategic suppliers and foundries to prioritize on healthcare supplies, directly working on component issues across all tiers of suppliers, diversifying sourcing of high-risk components with almost 400 alternate components certified to date. Lastly, we are also redesigning our printed circuit boards to qualify alternate sources of supply. Let me now provide guidance for certain areas of our business. In the segment Other, we expect a net cost of around 30 million euros at the EBITDA level in the fourth quarter, mainly due to the restructuring costs we mentioned. This means we expect an adjusted EBITDA of around zero in Q4 in this segment. We currently expect an effective tax rate of mid-single digit in 2022, We expect to deliver a positive free cash flow of around 600 million in the fourth quarter due to phasing of sales and working capital. In the full year 2022, we therefore expect a free cash outflow of around 700 million due to the lower earnings, temporarily higher inventories and the cash costs related to restructuring. In addition to measures to manage cash, we are taking measures to further strengthen our near-term liquidity position until we deliver on our order book and consequently start to see better cash flow from operating activities next year. In this context, it's important to clarify that we remain committed to dividend stability, which is an important part of our capital allocation policy. We secured a 1 billion euro credit facility to be used if and as needed and we will execute the settlement of forward contracts entered into as part of share repurchase program announced in July 2021 at the original settlement dates of 2023 and 2024 instead of in 2022 as previously announced. The forward Contracts with settlement dates in Q4-22 will be settled this quarter as planned. To wrap up, looking ahead, we see prolonged operational and supply chain challenges, a worsening macroeconomic environment, and continued uncertainty related to COVID-19 measures in China, which will be partly offset by our productivity and pricing actions. As announced on October 12, we now expect A mid single digit comparable sales decline in the fourth quarter of 2022 with a high single to low double digit adjusted EBITDA margin. We are actively monitoring the situation and our teams are working very hard on delivering on our order book and mitigating the impacts of headwinds. And we remain laser focused on our improvement actions. With that, I'd like to open the line for questions.

Thank you, sir. If any participant would like to ask a question, please press the star followed by two times one on your telephone. Due to the time, please limit yourself to one question. This will give more people the opportunity to ask questions. There'll be a short pause while participants register for questions. We will take our first question. Please stand by. And your first question comes from Hassan Alwakil from Barclays. Please go ahead. Your line is open.

Thank you for taking my questions. I have two, please. Firstly, to start with a high level question for Roy. Could you give us some insight about how you look to improve execution and set realistic and achievable targets going forward? I know Abhijit has talked about stretch targets in the past, which were in the midst of a transformation, and your view on the extent of supply chain shortages easing may have been overly ambitious in hindsight. But how should we think about the base case into next year? More specifically, what could revenue growth look like if you are unconstrained by supply and what could it look like if supply does not improve and would this impact the most profitable businesses? And then secondly, could you talk a bit about leverage and liquidity and how you think about the maintenance of the cash portion of the dividend given the deterioration in business performance and litigation Which, albeit, is likely a few years out in terms of potential payments. Could it make more sense to invest this incrementally into the business? Thank you.

Thank you, Hassan, for your question. Let me take the first one and then I can ask Abhijit to address the second one. So in terms of my insights, and as I've also shared, we have a very strong order book, but we have a serious challenge in conversion. and that challenge indeed is coming out of execution where we need to focus more in addressing the supply chain issues that we have with external suppliers, meaning we need to go to the next level of the second, third and fourth tier suppliers to secure the components that we need to get to complete our products so that we can bring them to installation. But also we need to improve our internal supply chain Agility, so we can deal better with the volatility that we see. For example, in redesigning part of the boards, but also improving the information flow that needs to flow seamlessly and fast from what we get on the supply side up to what we get from the customer side. So that's also when you heard me talk about the focus on execution, I very much look at quality, supply, and productivity to actually improve near-term our performance trajectory. and on that indeed I've also been talking about realism. Realism in terms of situations we face so that we can actually address the right areas to improve our performance trajectory but also secondly in terms of being realistic in terms of what the trajectory will be. Now as you can imagine I'm now my ninth day into the job and I will go into looking at the structural trajectory and also interventions that we're going to do and update you in January on the plan for 2023 and also the trajectory moving forward because we have a very strong portfolio. We have an exciting trajectory ahead, but we need to get our execution in line with the order book and with the potential that we have.

Thanks, Roy. Hassan, hi. Regarding leverage and liquidity, I think, look, our cash earnings this year have been lower Our inventories have been temporarily higher. So therefore, we have taken a term loan. So this is not a bond, multi-year bond. We've taken a term loan to help us go through this period because we will also have restructuring costs as part of the reduction in the people that we have spoken about. So as far as liquidity is concerned, we are not particularly concerned. We have adequate reserves and a strong balance sheet. And as I mentioned, you know, our commitment to dividend remains, so there should be no kind of concern on that front.

Thanks. And if I could just follow up on the question, just trying to understand, you know, a potential upside and downside scenario into next year with regards to supply, i.e., you know, given the order backlog that you have and if you were indeed unconstrained by supply, what that would look like. and what the business could look like in terms of no real improvement in supply and would this impact the most profitable businesses?

Yeah, I think, Hasan, as Roy mentioned, those are things that we are working through in the coming months. So I think we best leave that in terms of projections for next year to the update in January. We have a big, quick Q4 to deliver. I think we need to deliver on that and then we come back on how we see next year developing.

Maybe one color that we can give. If we would have an unconstrained supply for MR, we could deliver over one year of plan into the market. So that's kind of, I think, giving you a bit of color in terms of that actually we have a real strong order book where for some of our solutions, We have what we would normally sell in a year as part of order, but we need to unlock the supply to actually fully capitalize on that.

Yes, and that's across other modalities as well, you know, including IGT, etc. So you will see that our coverage for next year remains pretty high.

That's helpful. Thank you.

Thank you. We will now go to our next question. Please stand by. Your next question comes from the line of Veronica Duvojova from Citi. Please state your question.

Hi guys, good morning and thank you for taking my questions. I have two please. One, we'd love to understand how that 4,000 personnel reduction is spread across the various businesses and functions if you can give us M.D. Ph.D. Ph.D. Efficiency of R&D while reducing the absolute spend. And I'd just love to understand the logic and the rationale behind that and how confident are you that you can get more for less or at least the same amount of output for less. I think there's been some concerns around this by some of your large shareholders, so it would be good to understand how you're thinking through that. Thank you.

Thank you, Veronica. So let me address the first question. So in terms of the reduction in force, actually, it's a global measure we take. So actually, we will have and see impact across our operations globally. But of course, you will see that the highest impact is in our top four markets in terms of our entry base, which would be the US on top, then the Netherlands, and then India and China. So those is where we have the biggest absolute numbers, but that's also in line with the numbers of total workforce. Next to that, of course, we also are targeting first and foremost more group and staff functions, and we are protecting the operational access, of course, to ensure that we can deliver with quality and have all our manufacturing, operational, supply, service and sales staff fully focused on that. So that's how we drive the efficiency. And then on the second question in terms of innovation, yes, I do believe that we have room to improve our efficiency and effectiveness of innovation. And actually the view that I hold is that actually by focusing more on where we have strong innovation potential, but also skill potential, actually we get better returns for the investments that we are making. You saw that we have got some of the projects. Now, those are projects that would fit into that bucket, where actually we see that they would generate maybe less scalable big impact. So we are focusing now on fewer innovations that we can scale to a bigger size, but also ensure then that we do it at the right quality norm.

That's helpful. And Roy, if I can follow up on the reductions, Is there a specific business or area that you're targeting the most?

No, you have seen, and maybe it was called out, that we are going through our portfolio. So actually we see that we have this opportunity to start also with the tail end of smaller projects that we have across businesses. So we also look at it across countries in terms of where do we see the biggest And of course, this is also guided by what we get from our customers. So actually the customer pool and kind of where we see the orders coming in and demand being the strongest, of course, will fuel up more demand. I'm further working through also the structural measures. So as I said, I will come back to that in January in terms of where we're going to focus more to double down to generate an acceleration of our growth trajectory.

Okay. That's very helpful.

Thanks so much. Thank you. Your next question comes from the line of David Adlington from J.P. Morgan. Please go ahead and ask your question.

Morning, guys. First one on personal health care. I just wondered if you could help us out with I think we were expecting at least the outcome of the compatibility study. Just wanted to work any updates on that, please. Okay, maybe let me take the first one, David, and then, Roy, maybe you take the one on testing. Yep.

Overall, you've seen that the personal health demand in Q3 has held up pretty well. We had good growth in Western Europe, strong growth in North America. But going forward, with all the issues around energy pricing and lower customer confidence, we expect China to get softer in Q4. We expect Europe to get softer as well, whereas North America continues to remain strong. So let's say going forward into Q4, we are a bit cautious about our personal health business probably be in a kind of flat to slightly declining range. That is largely driven by consumer demand more than really any issue with our portfolio or supplies.

And then maybe on the testing. As you know, we have been coming forward with our test results that actually showed very encouraging results in December based on the VUC that were within standard. And then in June, where we reported back on the very low prevalence of foam degradation that we saw coming back from the devices that we tested. We are further testing, as we also shared. We are working through those also in collaboration with the regulators. So we unfortunately cannot share further detail now, but I promise you that the moment we can, we will be coming forth with those results immediately. Any calls in terms of when that might be, Roy? It's hard to predict, as I said, because it's not fully dependent on when we have completed, but also when we then work through with the various parties that are looking at it from an external perspective. So unfortunately, I cannot give you a date. I can only promise you that we are as eager as you to kind of conclude these and get these out. So the moment we can, we will inform you immediately.

Thank you. We will go to the next question. And the next question comes from Graham Doyle from UBS. Please go ahead and ask your question.

Good morning. Thank you for taking my question. First one just around supply chain. When you think of the issues you've had for the last, I suppose, over 12 months now, it doesn't feel like any of them are getting particularly better. But when we look at things like chip availability or freight rates, they certainly have been improving. What do you think is causing your particular issue? Is it maybe too much outsourcing or sort of a lack of foresight in terms of systems telling you where and when you're having these problems? And then a second question just around sort of follow up to Dave's question on the data. On biocompatibility, are you actually getting this data in-house on a regular basis and therefore have a sort of view on that? And then in relation to that, I know over the summer, Franz mentioned a number of around 50,000 individuals who have contacted a lawyer in relation to the litigation. I'm just wondering, have you got an update on that number as well, please? Thank you.

Okay, thank you, Graeme. Let me start with the supply chain. I think there are two parts of your question. One, do we see it getting better? So I think you heard Abhijit just talk about Ph.D. Ph.D. Ph.D. Ph.D. Our supply market that we need to source from. So we still have shortage of components, whether chips, whether batteries. But unfortunately also in second and third tier. We have improved quite significantly in the first tier suppliers. So actually we are last year around this time we will be looking at around 200 first tier suppliers that were very constrained. Currently it's around 20. But even if you have 20 constrained, it means that only one part missing and you cannot complete an installation. and therefore cannot bring it to the customer and not recognize. So it takes longer. Secondly, as I mentioned, there are also internal challenges that we need to address. The redesign of our products to more current components is something that we're working hard on. Also there we have made progress, but reality is also in a regulatory market that takes some time, especially with our current strong focus on quality. We also want to do it first time, right? and we have quite a significant amount of products to work through. Secondly, the information flow indeed, as I called out, is something that we are investing in to improve it, to just improve our agility, to address the volatility in the market better across the different product lines that we have. So whilst we see improvements and also you call out, for example, trades we expect to get better and logistics towards next year, We still see that we need to work through quite significantly on that. And on the second question, biocompatibility, yes, we have a lot of testing ongoing. Actually, it's internal, but also very much external, because we want to ensure that we have the external validation coming in. So that's actually continuously a dual program. But it's, as I said, not yet at a stage that we can share the outcomes. On the litigation side, we have currently around still a registered amount of 50,000 to 60,000 this time. So it has indeed increased a bit. We also have started now some of these processes in the market where the science day is starting. So you see the first kind of dialogues starting. But as we also shared before, it's too early to kind of predict any outcome of it. So we will come back when we have further news on that, but it's indeed true that we increased a bit in the number there.

That's great. Thank you. Maybe just one quick follow-up on biocompatibility. Could you just maybe explain or put some background in terms of the actual parameters and the testing that you have asked the third party to do? So how much input has the FDA said? Has it been, here's a standardized test we'd expect you to do, or have you designed these protocols from scratch?

So of course there are standards in the market that you have to comply with. So that's the first guidance that we put our testing towards. Secondly, you rightly say that we are in constant dialogue with the FDA as well and to kind of look at the testing protocols that we use. They also have actually continuous input from our side on our testing data. So actually we share the data that become available on a regular basis with them so they in essence have access to those data and then also give their views on it so this is a process that is in collaboration with the FDA but also with other regulators because they are also very interested of course in in this so so it's a combination of the standards that we test again but also if you have additional testing that we do we will share protocols that we use for feedback great thank you very much thank you

We will now go to our next question. And the next question comes from James Van Tempest from Jefferies. Please ask your question.

Hi, good morning. Thanks for taking my question. Just firstly on R&D, you mentioned shifting to fewer high-impact innovations, which I guess increases the R&D concentration risk and makes the timing of launches more lumpy. Just looking at the €120 million write-down in D&T, can you give us some examples of the types of innovation which have been shelved and what you'd consider higher impact and how this impacts the timing of launching new innovations? And then my second question is just on cash flow. You talked in Q3 about the consumption of provisions impacting operating cash flow. Just wondering what we can expect on that in Q4, and given your restructuring plans, can you give us a sense of where leverage is expected to land at the end of the year? Thank you.

Thank you James. So maybe starting off with the R&D question and Abhijit can take the second one. So if we look at a concentration risk that you mentioned, I would say that we have been more looking at innovation that was in the pipeline that actually was more fragmented, is further out and indeed doesn't generate the impact on scale that we expect from some of the innovations that we have currently in the market and that is working. So it's something that we have been looking at as part of keeping our innovation funnel healthy, making it stronger, and actually choosing the ones that have a better productivity and a better return rate. Examples of great innovations that we are further doubling down on are, for example, the MR Helium Free Next Generation, Informatics as part of our IGT solutions, but also our monitoring solutions where we see actually even more in the current market where demand is going and stepping also much more across and outside of hospitals to ambulatory and home situations. We see a significant opportunity there that we are further rallying around. So we're making choices that are M.D. Ph.D. Ph.D.

We will expect about a couple of hundred million, and this is when you say out of the provision, there are two parts. One is on the recall action, the other is on restructuring. So if you take both of them, that would be maybe close to between three to 350 million in the fourth quarter. In terms of leverage, we will not be significantly higher than where we are now. And that's why I said we have taken this more as caution to see that we have enough liquidity because the cash conversion of our inventories has pushed to next year. And that's why I said, you know, fourth quarter will have a positive free cash flow of 600 million because it is Normally a much bigger quarter, but this time we will have, let's say we've taken lower sales in our outlook and therefore slightly lower cash flow.

Thank you. And just to clarify one of the earlier points, so on the R&D then it sounds as if it's more about focusing resources and what can deliver innovation in the short term and sort of the medium to longer term initiatives are perhaps on the back burner for now until the business recovers. Is that a fair way to summarize that?

Now I think we are improving, we're looking at the funnel and I think we have room to kind of strengthen the funnel in terms of where we believe the biggest impact will be in the leadership positions and with exciting outlook. I think there is also common practice in terms of what you do in pruning your funnel continuously. And let's not forget that actually our R&D spend still is actually very significant with a 9 to 10% across the company. So it's not that we are straight away cutting to the bone. We are not slowing down. We want to accelerate the ones that we have in the pipeline where we see the better prospect and the better return profile.

Yeah, so it's not about short-term versus long-term. It's really investing and resourcing our bigger wins more than we've done in the past.

Thank you.

Thank you. We'll now go to our next question. And your question comes from Wim Gill from ABN Amro Odo. Please ask your question. Hello Wim, is your phone on mute? As there is no response, I will go to the next question. Please stand by. Your next question comes from the line of Falco Friedrichs from Deutsche Bank. Please go ahead and ask your question.

Thank you very much. Good morning. My first question is on the targeted annualized savings of 300 million. So when do you expect to reach that level? And related to that, what is the expected net impact next year, considering wage inflation and all of the other inflationary pressure? And then my second one is a quick follow-up on these conclusive test results. Understandable that you don't want to commit to a specific date, but is it fair to assume that we should get these test results this year still? Thank you.

Hi, Falco. Let me take first the targeted savings. That is the annualized savings, right? We plan to have most of the restructuring action completed by the end of the first quarter. So then you would probably get something like $200 to $225 million in the savings for next year. That would be the impact for next year as I see it. Regarding the testing, maybe I give that to Roy.

Yeah, Falco, we have, of course, all intent to do it as soon as possible. We need to do it right. We need to have it aligned. So therefore, I cannot commit to a date. Of course, I would love to see this year happening. But yeah, we'll have to keep you informed from the moment that we kind of can share the results.

Okay, thank you.

Thank you. Your next question comes from the line of Sezki Ozerna from HSBC. Please go ahead. Your line is open.

Good morning. Thanks for taking my questions. I have three, please. First of all, the 1.3 billion goodwill impairment, can you help us deconstruct that in terms of how much of that is coming from the estimated impact of the Constance Decree? and how much is coming from the change in the discount rate. My second question is I've seen the settlement dates for the forward share purchase transactions have been pushed into 2023 and 4 from 2022 while dividend commitment is maintained and also couldn't help but notice that the cash figure declined significantly Somewhat by third quarter. So I also appreciate that you have the $1 billion additional facility, but what are your plans and how much of the recall costs are completed? I see $4 million out of $5 million, $5.5 million devices were produced, but how much further costs do you estimate from that? And a final one as a follow-up, please. Do you expect the 4,000 FTE reduction to fully come from the existing businesses, or does it include any exits or divestments? Do you have that on the plan?

Yeah, so maybe going to the first one first, About a fifth, so about 20% of the impairment comes because of the change in the weighted average cost of capital. The rest comes from assumptions that we have made in terms of lower cash flow from the business going forward with potential actions that could be required by the FDA as part of the present decree. Now those are our best estimates at this point of time. And since we are in discussions with the FDA, it becomes very difficult to make those public at this time. So once we have that signed, we will, of course, make it public. Now, regarding the settlement dates of the forwards, you know, most of them, so I think about 80 million or so comes in Q4, which we will settle. And then most of it comes next year. So about 75% of the balance comes next year. and then the remaining part, the 25% is in 2023. So it's not pushed out. It is just earlier we had planned to pull it into this year and that was in the first quarter. We are just going back to the original dates that were committed. So we are not pushing it out. As far as the recall provision is concerned, currently we don't see The need to increase the provision, we have been utilizing it and by the end of the year, we would have, as Roy mentioned, complete 90% of the recall. The use of the provision may be a bit lower than 90%, but as the last pieces of the remediation is done next year, we will complete the use. But right now, we don't see any need for increasing that provision. Regarding the people, they largely come from existing businesses. They are not related to any divestment, so let me make that clear. There could be some smaller, really smaller businesses which we stop, but it's not a divestment. It's a very, very small, I'm talking about the 10s or 20 million annual revenue kind of thing. So that's how you should look at comes primarily from existing setup that we have today.

Thanks a lot. And if I may follow up the reduced revenue expectation, reduced cash flow expectation, which is related to goodwill impairment in this segment. Does this have to do also with the R&D projects that are being

Thank you.

Thank you. We'll go to our next question. And the question comes from Wim Gill from ABN, Amro Odo. Please ask your question.

Yes, good morning. Sorry for the previous term because I was kicked off the line accidentally. I have a question on the headcount reduction. In the Dutch press you mentioned that you will see in the Netherlands 400 forced reductions on a total employee base of 11,000. And on top of that you will see 400, let's say, natural attrition. So in total 800 reduction in M.D. M.D. Ph.D. 7,500 to 8,000 natural attrition people leaving the firm. How should we look at, let's say, hiring at Philips at the moment? Or how should we look at the total employee base in the coming, whatever, one, two years, given the structural headwinds that we're facing? Thanks.

Thank you Wim. Maybe let me take it. In terms of the foreign force layoffs, that's indeed true. You mentioned the order form coming out of attrition. I think that's too small of a definition. We will look also at temporary force to actually take into that account. So that's also where you see the difference with the 10% of attrition. So attrition of course will be looked at and used for outflow, but also we will reduce temporary workers. So if you compare the 800, that's indeed the comparable number, 44,000. And then we look at a global base, kind of how we exactly populate that. We also work through the different country structures and the local regulations and the workers' councils, et cetera, that will be involved. So this will be done in a proper manner. But the compare you need to make, 800 to 4,000, and then there's also temporary labor in that. Secondly, we will of course also make sure that we have a hiring reduction and therefore we will be very careful in hiring when we also exit people. At the same time, we will continue to upgrade and where we need to have capability injection or where we need to have specific expertise, of course we will hire that into the market. So I think we will be cautious, but we will not go into a full stop. Because we will continue to support the business with the needs in specific expertise areas.

So to be clear there, in the last three years your headcount increased every single year, whereas your top line did not increase accordingly. So will we have a better balance in the coming, let's say, one, two years with, let's say, the total headcount of the company compared to the top line development?

Yeah, I think we... So if you look to the headcount development, I think it was not a full life-for-life repair because we also have acquired companies, as you know, so I think we need to look at life-for-life. But at the same time, I think it's obvious that now with several quarters of decline We also need to decline the amount of people in line with that. We also signaled that this is an immediate initial action. I will be looking at the further plans and come back to you in January in terms of how we fully capture the potential of Philips based upon what we see outside as kind of the market and demand for our solutions, but also what is then the appropriate Thank you very much.

Thank you. We'll take our next question. And the question comes from Ed Ridley Day from Redburn. Please go ahead and ask your question.

Good morning. Thank you. Firstly, Thanks for the clarity on your restructuring initiatives. If we look at the safety and quality control process and the investment in restructuring, you're looking at the focus you would like to bring there. Roy, could you just give us a little bit more detail about how you envision improving that process, where particularly you might invest? Are you looking to bring in also senior hires perhaps from other medtech companies? Because clearly that is an area where Philips N.V. N.V. N.V. Thank you, Ed. Let me start with patient safety and quality. Indeed, as I outlined, we have

and I have put a lot of focus on improving execution because execution will help us to convert our order book and therefore realize better results and doing that firstly starts with indeed right focus on patient safety and quality. What we are doing there and where we will be also further deepening the effort is as you rightly call out of course there is a capability and culture question that we are addressing which means that we have been Thank you very much. Secondly, we're looking very strongly at the product portfolio that is in strong demand for the future and how we actually make that the best quality portfolio that we have. So that's something that we will also come back to in the January plan, which are the focus areas and how we're going to address that. If you look to the current quality regulatory team, just as a data point, At the group level, we have actually 70% new executives, all coming from MedTech. So if you look at the team of Francis Kim, who's leading that for us currently, he has assembled a team that comes from Stryker, Medtronic, Abbott, Pfizer, Boston Sci. So we're really assembling a very experienced team of quality and regulatory professionals. That actually will help us to actually step up in this area. So that's a big area of focus that we will continue to double down on. And then on the bigger picture asset, I will come back in January on my exact view on that, including which are the areas that we see the biggest growth and potential in the market, which are the segments where we see the demand going, and how are we lined up with our leadership positions to actually Capture that potential, which are the focus areas that we will go after. So then I will come back to that question and that will then look at the products, the portfolio, the full set of kind of how we intend to win in the market moving forward. Because we have a great potential asset, we have a great order book and we want to create even more impact. So that will be part of the plan that I will present in January to all of you.

Great, thank you.

Thank you. The last question comes from Robert Davies from Morgan Stanley. Please state your question.

Good morning. Thank you for taking my questions. I had a couple. One was on just the diagnostic and treatment business. Could you give us a little bit more color in terms of where you're seeing the relative strengths and weaknesses within that? N.V. N.V. N.V. N.V. Robert, let me take that. I think overall in diagnosis and treatment, we are, as I also mentioned earlier, we are doing extremely strongly in MR.

Roy mentioned that as well that you know the order book is so long that we will even not be able to supply it all next year. I think in image guided therapy that is our forte and there also we have been continuing to grow market share and size. The other one we talked about was informatics. I think there also we are growing extremely strongly. Actually, our ultrasound business order intake remains extremely strong. It's very unfortunate that due to a couple of components that we are not able to deliver, but as we start next year, our backlog for ultrasound is probably two and a half times what it is normally at the start of a year. So, I think across these modalities, we We see strong growth and probably in the area of CT we remain flattish. So that's how I would complete the whole look. On the CC margin decline, unfortunately it's a strong decline so it's important to explain it. There are two big factors. One is the decline in hospital patient monitoring and I think there's You will see a good recovery in Q4 as we kind of are able to deliver more. It's a high gross margin business and if you don't deliver, unfortunately you have all your fixed costs which hit the P&L. And secondly, in the sleep and respiratory business, we have had lower sales in masks in this quarter. That's a high margin part of our portfolio, so that hits us a bit. There were a couple of supply stops that we had for quality-related issues, which we have spoken about earlier, that also hits us a bit in this quarter. You will see connected care margins improving in the fourth quarter, but this quarter was hit heavily because of the reasons I just gave.

That's great. Thanks, both.

If no further questions, shall we check? Yeah.

Thank you.

Do we have any further questions?

Thank you. There are no further questions. I will hand back to you.

Okay. Thank you, operator. So thank you all for dialing in. We appreciate the opportunity to engage. As we started, we have a disappointing Q3 behind us, a challenging outlook, but a very strong order book. We're taking immediate and decisive measures to improve quality, improve supply chain, and improve productivity. We will stay on that to actually go back to delivery profile of quarter-over-quarter improvement. And I look forward to come back to you with a more comprehensive plan at the Q4 results. Also, a big thank you, of course, for all our employees for putting all their effort in this and also for going through a difficult moment. because we did announce head restructuring which is impactful as you can imagine. It's a very necessary measure we need to take but of course it hurts every single affected employee and all of us. So thank you for your attendance. Any further questions you will know how to find us also through our ER channel. Look forward to continue to engage with you. Thank you all.

Thank you. Thank you for participating. You may now disconnect.