Training Programs
All training programmes are delivered through SQT. And are tailored to cater for company specific requirements.
Cleanroom
- Controlling Contamination within the Cleanroom
- Effective Cleaning of a Cleanroom
- Cleanroom Microbiology
GMP
- GMP for Manufacturers of APIs
- GMP for Finished Pharmaceuticals
Medical Device
- ISO 13485:2016
- Medical Device Regulation (CE Marking Process & Key Updates)
- FDA 21CFR820 QSR & QSIT
Auditing
- Internal Quality Auditing for Manufacturers of API’s
- Internal Quality Auditing for Manufacturers of Finished Pharmaceuticals
- Internal Quality Auditing for Manufacturers of Medical Devices
- Internal Quality Auditing for Laboratories (ISO 17025)
- Internal Quality Auditing for Medical Laboratories (ISO 15189)
Laboratory
- Good Laboratory Practice (ISO 17025)
- QMS for Medical Laboratories (ISO 15189)