• Review of Excipient Specifications for release (routine controls) based on compendial monographs (European Pharmacopoeia, USP …) or supplier’s specifications
  • Review of Excipient supplier’s documentation for registration file (technical documentation, TSE/BSE, GMO certificates …)
  • Review of Packaging Specifications for release (routine controls) based on supplier’s documentation
  • Review of Packaging supplier’s documentation (technical documentation, drawings)