PHATOPHY - Drugs Study in Animal

- PHATOPHY recruits a Study Director for the in-life phase department

 

- PHATOPHY is Level A GLP certified since August 2010 

 

- PHATOPHY celebrates its 30 years and reported it through an article on the "Gazette du Laboratoire"

Four persons are responsible for ensuring regulatory evolution in their respective areas to analyze the draft versions in preparation and implementation of new guidelines

 

They are also involved on this in:

 

-discussions with agencies and advice for developing your products

 

-writing of parts I, II, III and IV of the MA dossiers of the veterinary medicinal drugs

 

-writing MRLs files or extension for MRLs

 

-writing records of variations

 

-writing export files in accordance with European requirements (NTA format) or other (CTD format).