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Blog

Blog Medical Devices

Medical Devices

Beyond Europe: The Strategic Value of CERs in FDA Submissions

14 May, 2025

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

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Medical Devices

Join Celegence at RAPS Euro Convergence 2025

16 Apr, 2025

Blog Pharmaceutical

Pharmaceutical

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

Pharmaceuticals

Regulatory Publishing

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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Austrian Agency for Health and Food Safety (AGES)

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Agency for medicinal products and medical devices of Croatia (HALMED)

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Ministry of Health – Pharmaceutical Services

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State Institute for Drug Control (SUKL)

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Danish Medicines Agency (DKMA)

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State Agency of Medicines (Ravimiamet)

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Finnish Medicines Agency (FIMEA)

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National Agency for the Safety of Medicine and Health Products (ANSM)

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German Institute of Medical Documentation and Information

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Beyond Compliance: Preparing for IDMP Now and Into the Future

November 16, 2025 | Online

Pharmaceutical

Webinar

Beyond Compliance: Preparing for IDMP Now and Into the Future

DIA 2022 Global Annual Meeting June 20-22

June 20, 2025 , Chicago, IL

Event

Pharmaceuticals

DIA 2022 Global Annual Meeting June 20-22

Staying Compliant: Strategies for EU MDR and Beyond

May 22, 2025 | Online

Medical Devices

Webinar

Staying Compliant: Strategies for EU MDR and Beyond

The Regulatory Landscape in 2025: What you need to know

May 7, 2025 | Online

Pharmaceutical

Webinar

The Regulatory Landscape in 2025: What you need to know

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

April 28, 2025 | Berlin , Germany

Event

Pharmaceuticals

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

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 2024

April 9, 2025 | Brussels

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Pharmaceuticals

Global Pharmaceutical Regulatory Affairs Summit – GPRAS 2024

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

How to Optimize the ROI on Your RIMS Solution Webinar

February 24, 2025 | Online

Pharmaceutical

Webinar

How to Optimize the ROI on Your RIMS Solution Webinar

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