The Compliance Group has long been associated with offering open and tailored training courses to the pharmaceutical community.
We have run courses such as Good Distribution Practice (GDP), Good Manufacturing Practice GMP, Pharmaceutical Auditing, Data Integrity, Mock Inspection, SME Mentoring, How to Inspect, Introduction to Regulatory Affairs, among others.
The following is our current offering of open training courses, and tailored course options, offered by The Compliance Group. If your course of interest is not currently scheduled, please contact us to inquire about the next scheduled date or about the possibility of running the course in-house.
good distribution practice
Good Distribution Practice (GDP) is the standard set down in European Directives to which wholesalers of medicinal products must comply. GDP forms the basis of the Quality Management System operated by wholesalers.The next course will be delivered over two sessions on consecutive days…
pharmaceutical auditing
Across the many diverse business functions within the pharmaceutical industry, the requirement to perform audits of key service and material suppliers has become a significant driver for regulatory Pharmaceutical Auditing compliance and corporate governance. This 6 day course, divided into 3 two day blocks, has been accredited by UCC School of Pharmacy
customised training
Where a specific course is not listed, we are always pleased to discuss the specific needs of our customers. Based on the customer wishes, we can bundle or modify existing services, or develop new services; always keeping in mind our desire to provide efficient and cost effective solutions.
bespoke courses
Where a specific course is not listed, we are always pleased to discuss the specific needs of our customers. Based on the customer wishes, we can bundle or modify existing services, or develop new services; always keeping in mind our desire to provide efficient and cost effective solutions.
Some previous custom courses include:
- Aseptic Fill Finish
- Benchmarking
- Contamination Control Strategy
- Data Integrity
- Deviation Training
- EU Clinical Trials Legislation
- EU Regulations and the role of the Qualified Person (QP)
- Forensic Auditing – Data Integrity
- Good Cleaning Validation Practice
- High Purity Water Systems
- Inspection responses
- Introduction to Reg Affairs
- Pharmaceutical Microbiology
- Sterilisation and Depyrogenation
