ARCexperts’ training services provide tools that help highly regulated companies prevent potential quality problems and make it easier to prove to FDA regulators that your quality standards and policies work. Training is required within the development or production stages of any regulated product in the life science industry and creating strategies that ensure professionals receive the training required is a significant task. Our experts deliver the information and data needed to reach compliance.

Our training services reach a wide-span of subjects including: 

  • Internal Auditing
  • All ISO Regulations
  • Quality Management Systems (QMS)
  • Medical Device Directive (MDR, MDD)
  • Standard Operation Procedures (SOP)
  • Good Manufacturing Practice (GMP)
  • Good Laboratory Practice (GLP)
  • Good Clinical Practice (GCP)
  • Process validation (IQ, OQ, PQ, TPQ)
  • Quality System Regulation (QSR)
  • Clinical Evaluation Reports (CER)
  • Computer Systems Validation (CSV) and other validation services