+44 (0)1933 357953 info@qualogy.co.uk


With the ever changing regulations within the Pharmaceutical and Research industry, keeping up to date with the regulations and providing evidence of the knowledge and training gained is imperative.

Our courses are designed to be interactive to aid the delegates, share experiences, and to understand the regulatory requirements that apply in your organisation.

All courses include workshops and encourage delegate discussions, plus a comprehensive set of course notes and a certificate of attendance.

The courses are designed to meet delegates training requirements and a company’s specific needs. 

We offer an extensive range of company in-house courses which include the following.

GCP Training

  • Introduction to GCP
  • Monitoring and Auditing Clinical Laboratories
  • GCP Compliance for Monitors
  • Advanced Quality Assurance
  • Good Clinical Laboratory Practice (GCLP)

GLP Courses

  • GLP Training for Test Facility Management
  • GLP Training for Study Directors and study staff
  • Conduct of Multi-site studies in compliance with GLP
  • Advanced Quality Assurance
  • Implementing GLP in your Company
  • Advanced GLP (the real issues)
  • GLP in the Laboratory

GCLP Training

Training courses are offered for staff working in laboratories that undertake the analysis of samples from clinical trials in the requirements, interpretation and application of GCLP. Courses are also offered to clinical trial monitors on the requirements to look for during the monitoring of clinical laboratories.

Those in the Middle

  • Management & Archiving GLP & GCP records
  • SOP Writing

Archive Training Courses

Annual courses are held in conjunction with The Scientific Archivists Group (SAG) at our Qualogy premises twice a year Managing and Archiving of Preclinical (GLP) and Clinical (GCP) Material


For futher details please contact us

By phone 01933 357 953

or by email info@qualogy.co.uk