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