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Blog

Blog Medical Devices

Medical Devices

EU MDR Clinical Evidence: Meeting the Mark for Regulatory Compliance

05 May, 2025

Pharmaceutical

Webinar Pharma

AI in Action: Tech-Empowerment in Medical and Technical Writing

29 Apr, 2025

Industry Conferences

Medical Device Industry Conferences

Medical Devices

Join Celegence at RAPS Euro Convergence 2025

16 Apr, 2025

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Mitigating Risks and Reducing Timelines in CMC for ATMPs & CGTs

10 Apr, 2025

Medical Devices

Webinar

Webinar Medical Devices

Staying Compliant: Strategies for EU MDR and Beyond

09 Apr, 2025

Blog Pharmaceutical

Pharmaceutical

IDMP Compliance for Pharma: Strategy & Benefits

08 Apr, 2025

Blog

Blog Medical Devices

Medical Devices

Enhancing Systematic Literature Reviews for Adverse Events with AI

03 Apr, 2025

Blog Pharmaceutical

Pharmaceutical

Key Takeaways From RSIDM Regulatory Forum 2025

31 Mar, 2025

Pharmaceutical

Webinar Pharma

The Regulatory Landscape in 2025: What you need to know

28 Mar, 2025

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IDMP Proof-of-Concept

25 Mar, 2025

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25 Mar, 2025

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Regulatory Readiness and Resources Survey Report 2024

Get instant access to the survey report that regulatory professionals are talking about: the 2024 RAPS & Celegence Regulatory & Readiness Survey.

Lean Authoring Checklist

Lean Authoring: Eliminating Redundancies And Complexities For The Pharmaceutical Industry And Health Authorities

EU Scientific Advice Whitepaper

Download our exclusive report to streamline regulatory approvals and optimize your EU scientific advice strategy.

The Burden of Brexit on the Medtech Industry: Whitepaper

The Burden of Brexit on the Medtech Industry: Whitepaper Make sure your organization is well versed and prepared for the implications of Brexit by reading Celegence’s White Paper examining the challenges and implications of compliance in the United Kingdom following Brexit.

Medical Device Regulatory Survey Report 2024

Be the first to explore pivotal findings that will shape the future of MedTech regulation. Our survey covered key topics such as current challenges, resource allocation, advanced technologies, and regulatory processes to provide a clear picture of where the industry is headed.

EU MDR Checklist

Make Sure You’re EU MDR Compliant As regulatory specialists, we are aware of the burden you are probably under in making your medical device business compliant with the upcoming EU MDR which comes into force later this year. As part of our commitment to helping businesses make the transition, we have compiled a checklist which […]

EU IVDR Checklist

Make Sure You’re EU IVDR Compliant As regulatory specialists, we are aware of the burden you are probably experiencing in making your In Vitro Diagnostic device compliant with the EU IVDR which comes into force next year. The EU IVDR affects all IVD medical devices and will bring about several major changes. As part of […]

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Ministry of Health – Pharmaceutical Services

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Regulatory Submissions, Information, and Document Management Forum (RSIDMF) 2025

February 3, 2025 | North Bethesda , MD

Event

Forum

Pharmaceuticals

Regulatory Submissions, Information, and Document Management Forum (RSIDMF) 2025

Global Pharmaceutical Regulatory Affairs Summit – GPRAS 2024

April 9, 2025 | Brussels

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Pharmaceuticals

Global Pharmaceutical Regulatory Affairs Summit – GPRAS 2024

10th Annual Master Data and Data Governance Excellence in Life Sciences – September 2024

September 19, 2024 | Berlin , Germany

Event

Pharmaceuticals

10th Annual Master Data and Data Governance Excellence in Life Sciences – September 2024

6th Annual Life Science Regulatory Intelligence & Strategy Conference

April 10, 2025 | Baltimore , Maryland

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Pharmaceuticals

6th Annual Life Science Regulatory Intelligence & Strategy Conference

Global Pharmaceutical Regulatory Affairs Summit (GPRAS 2023)

October 23, 2023 | Brussels , Belgium

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Pharmaceuticals

Global Pharmaceutical Regulatory Affairs Summit (GPRAS 2023)

9th Annual Master Data and Data Governance Excellence in Life Sciences – Sept 2023

April 28, 2025 | Berlin , Germany

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Pharmaceuticals

9th Annual Master Data and Data Governance Excellence in Life Sciences – Sept 2023

Regulatory Submissions, Information, and Document Management Forum (RSIDMF)

February 13, 2025 | North Bethesda , USA

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Pharmaceuticals

Regulatory Submissions, Information, and Document Management Forum (RSIDMF)

DIA 2022 Global Annual Meeting June 20-22

June 20, 2025 , Chicago, IL

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Pharmaceuticals

DIA 2022 Global Annual Meeting June 20-22

Celegence to Exhibit at MAPS Americas 2025 – Advancing AI in Medical Affairs

March 26, 2025 | New Orleans

Event

Medical Devices

Celegence to Exhibit at MAPS Americas 2025 – Advancing AI in Medical Affairs

11th Annual American Medical Device Summit 2024

October 1, 2024 | Chicago

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Medical Devices

11th Annual American Medical Device Summit 2024

RAPS Regulatory Convergence 2024

September 18, 2024 | USA

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Medical Devices

RAPS Regulatory Convergence 2024

RAPS Euro Convergence 2024

May 7, 2024 | Germany

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Medical Devices

RAPS Euro Convergence 2024

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