Training and Consultation

CONSULTATION IN REGULATORY SUBMISSION AND R&D

  • Product safety assessment (local and international) – USFDA 510K, Medical Device Authority (MDA), Pesticide Board, DOSH, NPRA
  • Product development
  • Histopathology slide observation

TRAINING

  • Quality system (ISO 17025, OECD GLP)
  • Animal husbandry
  • Cell culture handling
  • Biocompatibility evaluation as per ISO10993