Training

1
Quality system (ISO10725, OECD GLP)
2
Test method
3
Animal Handling
4
Cell culture handling

Consultation in regulatory submission and R&D

1
Product safety assessment (local and international) – US FDA 510k, Medical Device Authority, Pesticide Board, DOE, DOSH, NPRA
2
Product development
3
Histopathology slide observation
4
Biological Evaluation Report - Summary of Biocompatibility Test Reports