New levels of productivity and digitalization for the clinical lab
Diagnostics
Deepak Nath
President Laboratory Diagnostics
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Unrestricted © Siemens Healthineers, 2020
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Unrestricted © Siemens Healthineers, 2020
Diagnostics - Building from a leading position with the broadest portfolio in the industry
Strong positions …… in an attractive market …… with global scale
€28bn+ | >5% | 300k+ | 135+ | |||||
Laboratory Automation Point-of- | Market | Market | Global Installed | Number of | ||||
Diagnostics | Care | Size1 | CAGR1 | Base2 | Countries2 | |||
Decentralized settings | Centralized settings |
Connected point-of-care solutions
Workflow excellence
Clinical
excellence
Automated, high throughput solutions
Urinalysis | Blood Gas | Digitalization | Atellica Solution (CC/IA) | Automation/IT |
End-to-End Solutions |
HbA1C | Cardiac | Informatics | Hematology | Coagulation | Urinalysis |
3 | |||||
1 2019 BBC Annual IVD Market Book in USD and calendar year, excludes Molecular Diagnostics 2 Internal data | Unrestricted © Siemens Healthineers, 2020 |
Atellica® Solution delivers tangible value to customers | ||||||||||||||||||||||||||||||||||||||||||
(catalyst for growth) | Customized configurations | 33% | ||||||||||||||||||||||||||||||||||||||||
to meet individual lab needs | ||||||||||||||||||||||||||||||||||||||||||
fewer analyzers 4 | ||||||||||||||||||||||||||||||||||||||||||
>35% | Seamless | |||||||||||||||||||||||||||||||||||||||||
integration of | ||||||||||||||||||||||||||||||||||||||||||
Competitive wins | emergency and | |||||||||||||||||||||||||||||||||||||||||
routine testing | ||||||||||||||||||||||||||||||||||||||||||
86% | >80% | |||||||||||||||||||||||||||||||||||||||||
fewer operators4 | ||||||||||||||||||||||||||||||||||||||||||
Advanced automated workflow | Remote proactive | Mega Lab2 competitive | ||||||||||||||||||||||||||||||||||||||||
73% | Highest immunoassay | monitoring and support | win rate with TLA3 | |||||||||||||||||||||||||||||||||||||||
to reduce manual interventions | ||||||||||||||||||||||||||||||||||||||||||
productivity 1 | ||||||||||||||||||||||||||||||||||||||||||
less hands-on time 4
Designed to meet evolving
needs of customers…
+ |
…with good uptake
in the market…
= |
…and tangible
customer impact.
Product availability may vary from country to country and is subject to varying regulatory requirements
1) Based on tests per hour per m2 when compared to leading competitive modular immunoassay instrument 2) Labs processing in excess of ~30 k tubes/day
3) TLA = Total Lab Automation 4) The outcomes obtained by individual Siemens Healthineers customers were realized in the customers unique setting. Since there is no typical laboratory, and many variables exist, there can be no guarantee that others will achieve the same results Source: Laboratory Diagnostics
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Unrestricted © Siemens Healthineers, 2020
COVID-19 impacted performance - improvement expected in FY21
Grow Expand Elevate
Delivering on the promise of Atellica Solution
Development of adjusted EBIT | ||||||
margin (illustrative) | ||||||
FY19 | Volume | COVID-19 | Atellica | Other | FY20 | FY21 |
Performance in FY20 significantly impacted by COVID
- Severe decline in routine care testing, partial recovery in Q4
- Continued "investment" in service and maturing Atellica systems: foundational to margin improvement in FY21, high seeding rates for Atellica instruments
Outlook FY21: improvement expected in both top and bottom line
- Routine care recovers but remains below 2019 levels
- Good progress in maturing of Atellica platform
- Improved factory utilization
- Strengthened leadership team
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Unrestricted © Siemens Healthineers, 2020
Our portfolio innovations will deliver the lab of the future
Grow Expand Elevate
Workflow excellence
Clinical
excellence
Lead in workflow and achieve clinical excellence
Positioning ourselves for the future | Innovating in workflow | |
• | Deliver further Atellica innovations incl. Mid-Volume system (CI19001) | • Enhance and expand Atellica Solution IT |
• | Launch assays to continue menu enrichment | • Strengthen laboratory automation offerings |
1 In development. Future availability cannot be guaranteed.
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Unrestricted © Siemens Healthineers, 2020
Best-in-class testing for COVID-19
Total Antibody Assay: IgG/IgM** | Both tests are CE-marked and | ||||||||||||||||||
FDA EUA-authorized and run on | |||||||||||||||||||
• | 100% sensitivity, 99.8% specificity3 | one of largest installed base of | CoV-SARS | have I Do | |||||||||||||||
critical care tests for COVID-19 | • | Utilizes the spike protein to detect total | high-throughput automated | ||||||||||||||||
antibodies to block the virus entry into human cells | analyzers worldwide | ||||||||||||||||||
patients including | |||||||||||||||||||
25 D-Dimer,IL-6*, SAA*, CRP, | |||||||||||||||||||
IgG Quantitative Antibody Assay** | |||||||||||||||||||
19?-COVID | Procalcitonin (PCT), TnIH | • | 100% sensitivity, 99.9% specificity, 3 | ||||||||||||||||
• | Measures levels of IgG neutralizing antibodies | virus?2- | thetoantibodies | ||||||||||||||||
to the spike protein, enabling tracking of | |||||||||||||||||||
changes over time | |||||||||||||||||||
Molecular SARS-CoV-2 test kit** | |||||||||||||||||||
• FDA EUA-authorized,CE-marked, WHO EUL | |||||||||||||||||||
• 100% positive, 100% negative agreements1 | |||||||||||||||||||
have | |||||||||||||||||||
Rapid SARS-CoV-2 POC Antigen Test2 | |||||||||||||||||||
• CE-marked; under FDA review for EUA | |||||||||||||||||||
Do I | • Portable visual read, 15-min. TAT | ||||||||||||||||||
*Not available for sale in the U.S. | |||||||||||||||||||
**These SARS-CoV-2 molecular and serology tests have not been FDA cleared or approved. These tests have been authorized by FDA under an EUA for use by authorized laboratories. The molecular test has been authorized only | 5 | ||||||||||||||||||
for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The serology test has been authorized only for detecting the presence of antibodies against SARS-CoV-2, not for any other viruses or | |||||||||||||||||||
pathogens. These tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under |
Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. Product availability may vary from country to country and is subject to varying regulatory requirements.
1) In method comparison studies, FTD SARS-CoV-2 has shown Positive Percent Agreement: 100% (91.8-100, 95% CI) and Negative Percent Agreement: 100% (88.7-100, 95% CI) when tested in Copan eSwab nasopharyngeal and | |
oropharyngeal swabs. | |
2) CE-IVD labeled for diagnostic use in the EU. Research Use Only (RUO) in the U.S. | 7 |
3) For samples collected ≥14 days after positive PCR result. | |
5) www.thelancet.com Published online September 25, 2020 https://doi.org/10.1016/S0140-6736(20)32006-7 and Clarke C, Prendecki M, Dhutia A, et al. High prevalence of asymptomaticCOVID-19 infection in hemodialysis | Unrestricted © Siemens Healthineers, 2020 |
patients detected using serologic screening. J Am Soc Nephrol 2020; 31: 1969-75. Commentary from Barnaby Flower, Christina Atchison Department of Infectious Disease, Faculty of Medicine, Imperial College London |
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Siemens Healthineers AG published this content on 25 November 2020 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 30 November 2020 09:10:07 UTC