+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

 Qualogy offer Good Clinical Laboratory Pratice (GCLP) training courses for organisations and laboratories which process and analyse samples from Clinical Trials.

GCLP is the interpretation of those aspects in ICH GCP that apply to the laboratories involvement and contribution to Clinical Trials.

The training course can aid the laboratory to understand and apply the GCP requirements to their work.

Those in the Middle

  • Management & Archiving GLP & GCP records
  • SOP Writing

Archive Training Courses

Archive courses are held  at our Qualogy premises twice a year Managing and Archiving of Preclinical (GLP) and Clinical (GCP) Material

For further details please contact us at