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  - - Understanding the requirements and nuances of sterility testing
      
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      16th January 2025
      
      The Lifespan of Mature Drugs in 2025: Q&A with Kirsten Jacobs
      
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Webinars related to Agency Interactions

Webinar Know your market

Webinar

Know your market: US and EU regulatory expectations for combination products

4th April 2024

Ask an Expert

Webinar

Ask The Expert: Regulatory Agency meetings and Special Designations

6th December 2022

IRIS Webinar

Webinar

IRIS Portal – Scientific Advice, Orphan Designation, and i-SPOC application submissions to EMA

3rd November 2022

Webinar

eCTD in Australia: key steps to start a successful submission

28th June 2022

Webinar

Webinar

Software Medical Devices – Considerations for Regulatory Compliance Success

Webinar

Webinar

How technology optimizes the publishing process for regulatory submissions

Webinar

Webinar

Global framework of interactions with Heath Care Professionals : Loi anti-cadeaux in France

Webinar

Webinar

Basic rules of pharmaceutical advertising in France

Webinar

Webinar

US NDA versus EU MAA eCTDs – Exploiting the Synergies and Mastering the Differences

Webinar

Webinar

What you need to know to submit Study Data to FDA & what the new FDA Technical Rejection Criteria means for you

Webinar

Webinar

Central American Regulation for Drug Products (LATAM)

Webinar

Webinar

An Update to In Vitro Diagnostics Regulatory Requirements Worldwide

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Solutions

Strategic and Scientific Consultancy
Integrated Product Development
Innovations to Market
Optimal Patient Access
Business and Portfolio Mergers & Acquisitions

Strategic and Scientific Consultancy
Integrated Product Development
Innovations to Market
Optimal Patient Access
Business and Portfolio Mergers & Acquisitions

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