Skip to content

About Us
Solutions
- - - Industry Solutions
      
      Strategic and Scientific Consultancy
      
      Integrated Product Development
      
      Bringing Innovations to Market
      
      Post-launch Outsourcing
      
      Local Affiliate Services
      
      Business and Portfolio Mergers & Acquisitions
      
      Menu
      
      Industry Sectors
      
      Biotech
      
      Pharmaceutical & Consumer Health
      
      MedTech
      
      Menu
      
      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
  - - Achieving trial master file quality, timeliness and completeness
      
      Journal Article
      
      31st January 2023
      
      Managing the medical device pre-submission process with the FDA
      
      Podcast
      
      30th January 2023
      
      Countdown for EU health institutions using in-house devices
      
      Blog & Article
      
      30th January 2023
      
      Mark Lane | PharmaLex Expert
      
      Video
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

Menu

About Us
Corporate Social Responsibility
Sustainability
Management Team
Sectors

Useful links

Contact Us
Imprint
Data Protection
Terms and Conditions

Menu

Contact Us
Imprint
Data Protection
Terms and Conditions

Solutions

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

Menu

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

Newsletter Sign Up

SGS ISO9001 System Certification

©2023 PHARMALEX GMBH. ALL RIGHTS RESERVED.

Linkedin-in Youtube Twitter

Scroll to Top