Versions Compared

Old Version 5

changes.mady.by.user ZHATKIN Yurii

Saved on

compared with

New Version 6

changes.mady.by.user MONTARD Laurence

Saved on

Key

  • This line was added.
  • This line was removed.
  • Formatting was changed.

...

  • Evaluation of applications for certificates of suitability to the monographs of the European Pharmacopoeia and management of the inspection programme of manufacturing sites and associated brokers”.;
  • Planning, implementation and coordination of post-marketing surveillance studies for medicinal products and management of related databases;
  • Coordination of the elaboration and issuance of guidelines related to the OCABR procedure for the release of batches of human immunological medicinal products (blood and vaccines);
  • Management of the elaboration, revision, correction and suppression of European Pharmacopoeia texts, their publication in printed and electronic format and their distribution;
  • Conduct of laboratory studies

...