Our ”Training the Trainer Program” provides the implementation of a documentable training program, from operator level through management level personnel and meets U.S. and International professional and regulatory requirements.
Magid-Haffner Associates, Inc. offers customized training programs for pharmaceutical, biotech and device companies.
Our training programs cover:
Good Manufacturing Practice (GMP) for:
- APIs
- Drug product
- INDs
- ANDAs
- NDAs
- BLAs
- EU MAAs.
Good Clinical Practice (GCP) for:
- CTM (Clinical Trial Management) Services & Document Submission
- Packaging & labeling
- Clinical Monitoring
- Clinical QA Auditing
- Data Management
- Phase I – II – III Clinical services
Quality System Regulation (QSR)
- Medical Device
- In vitro Diagnostics