Skip to content

About Us
Solutions
- - - Industry Solutions
      
      Strategic and Scientific Consultancy
      
      Integrated Product Development
      
      Innovations to Market
      
      Post-launch Outsourcing
      
      Local Affiliate Services
      
      Business and Portfolio Mergers & Acquisitions
      
      Industry Sectors
      
      Biotech
      
      Pharmaceutical & Consumer Health
      
      MedTech
      
      Departments
      
      Services
      
      Research and Development
      
      Statistics and Data Science
      
      Market Access
      
      Patient Safety (Pharmacovigilance)
      
      Regulatory Affairs and CMC
      
      Quality Management and Compliance
      
      Training
      
      Research and Development
      
      Statistics and Data Science
      
      Market Access
      
      Patient Safety (Pharmacovigilance)
      
      Regulatory Affairs and CMC
      
      Quality Management and Compliance
Solutions
Insights
- - - News & Events
  - - Thought Leadership
  - - Assessing gaps and achieving compliance with Annex 1
      
      Podcast
      
      1st December 2023
      
      We are becoming Cencora PharmaLex
      
      Company News
      
      30th November 2023
      
      Preparing for device tracking: Next steps with Australia’s UDI
      
      Blog & Article
      
      16th November 2023
      
      New FDA Guidance Addresses Challenges with Cell and Gene Manufacturing Comparability and Complexity
      
      Journal Article
      
      6th November 2023
Insights
- News & Events
- Thought Leadership
Digital Innovation
Careers
Contact Us
Global Reach

Webinars related to Post-Approval Maintenance

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

Webinar

Electronic Submission in the EAEU – the challenges

« Previous Page1 Page2 Next »

Company

About Us
Corporate Social Responsibility
Sustainability
Management Team
Sectors

About Us
Corporate Social Responsibility
Sustainability
Management Team
Sectors

Useful links

Contact Us
Imprint
Data Protection
Terms and Conditions

Contact Us
Imprint
Data Protection
Terms and Conditions

Solutions

Strategic and Scientific Consultancy
Integrated Product Development
Innovations to Market
Post-launch Outsourcing
Local Affiliate Services
Business and Portfolio Mergers & Acquisitions

Strategic and Scientific Consultancy
Integrated Product Development
Innovations to Market
Post-launch Outsourcing
Local Affiliate Services
Business and Portfolio Mergers & Acquisitions

Newsletter Sign Up

©2023 PHARMALEX GMBH. ALL RIGHTS RESERVED.

Linkedin-in Youtube Twitter

Start typing and press enter to search

Search …

Scroll to Top