Training


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)