Europe (English)  Francaise  Italiano  Svenska  Dansk

Banner1int

 

Search

  

 

RSS feed RSS feed (English)

 

Home

 

International courses

Compliance Seminars®

Webinars

 

Courses in local languages

Français

Italiano

Svenska

Dansk

 

Literature

Collection of GMP's for pharmaceutical production

The GMP Handbook for pharmaceuticals

Quality Systems Handbook for MedDev

QSIT

Basic statistics for QC-Lab

ICH Q8, Q9, Q10

GMP translations (FR, IT, SE, DK)

 

Consulting

 

KEY2GMP®

Search tool and document library. Find you way in regulations, guides and other reference documents.

 

Newsletter

Subscribe / unsubscribe

 

Other

About us

Contact

Site map

Links

Course venues

Affiliates

Policys and Cookies

Dr Freddy Vaede, Ph.D.

Senior Consultant in GMP and Quality Matters

 

Dr. Freddy Vaede has 35 years of experience in the Pharmaceutical Industries with multinational companies in various positions of Quality Department. With an Industrial Pharmacist background from Paris University and a specialization in Analytical Chemistry, he was first and for 15 years Head of Quality in 2 dosage form manufacturing sites (ICI-Phama now Astra-Zeneca and Rhône-Poulenc now Sanofi-Aventis) before he joins Corporate positions in Quality Department of Rhône-Poulenc Rorer then Aventis and finally Sanofi-Aventis. His last position in Sanofi-Aventis was Director Strategic Support in Corporate Quality Department.

 

During his long career Mr Freddy Vaede has developed his competency and expertise in GMP and Quality matters on Active Pharmaceutical Ingredients (ICH Q7A) and Dosage Forms (21CFR parts 210 & 211 and European GMP’s). He was specialized in supporting on GMP manufacturing sites located in Europe and Asia (India, China, Japan, Singapore), in assisting them efficiently at the shop flour level in their preparation to FDA and European Authorities Inspections and in managing these inspections where needed as a facilitator. He has a long list of successful results on these supports.

 

Mr Freddy Vaede has participated actively in the preparation of Corporate Quality and GMP Guidelines/Standards for Rhône-Poulenc Rorer, Aventis and then Sanofi-Aventis. Among his other various responsibilities, Mr Freddy Vaede was also in charge of a tremendous number of audits performed in API’s, Dosage Forms and Sub-contractors manufacturing sites located worldwide (Europe, Asia, USA). He was also responsible to manage quality risks for API’s from biological origins (Heparins and others) such as viral safety, BSE, etc.

 

Mr Freddy Vaede was a Qualified Person in Rhône-Poulenc Group, an analytical expert for French Health Ministry and is a Certified APIC auditor.

 

During the last 3 years Dr Freddy Vaede has worked as a Senior Consultant for several US, European and Asian companies.

 

Our courses with Dr Freddy Vaede:

» Handling foreign inspections in a multicultural environment #5107

Banner2int