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      18th September 2025
      
      Establishing a therapy’s market access and commercial potential with early phase modeling
      
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Webinars related to eCTD, System Operations and Data Management

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

Webinar

Biotech Drug Development Challenges and Case Studies (CMC)

Webinar

eCTD in China

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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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