Group training at your site (or one of our offsite centers) is a great solution to kick start a new initiative or to offer customized GMP training that is aligned with company objectives while staying within financial constraints. It’s the ideal solution if you have four or more people to be trained.

CiPharma’s training courses can be delivered anywhere in the world. If your site is not in a city we have an office in then we ask you to cover the travel costs from our nearest office. You’ll save the costs associated with your staff traveling to be trained, so it becomes cost effective if you have several people needing train.

Our GMP training courses include:

Audit success

The course is designed both for people with internal auditing responsibilities within a company and for those who want to understand how the regulatory audit process works and how to be prepared for an external audit.

Good Manufacturing Practice (GMP)

This course is designed for people who are new to a GMP regulated environment or need a refresher in the latest GMP changes. It covers the current PIC/S and FDA GMP guidelines.

Good Documentation Practice (GDP)

This Good Documentation Practice (GDP) course provides participants with the skills to write clear, concise procedures and validation protocols.

Good Laboratory Practice (GLP)

This course is designed for people working in the early phase drug development and commercial operations. The course is updated regularly to provide participants with current GLP trends and information.

Computer System Validation

This course is designed for people who need an introduction to computer system validation within a GMP-regulated industry.

Process Validation

This course is designed to provide an overview of the latest concepts and guidance documents for Process Validation.

GAMP5 and computerised systems compliance

This course covers the essential principles contained in GAMP 5: A Risk Based Approach to Compliant GxP Computer Systems Validation. This GAMP course is designed for professionals seeking training in the requirements of GAMP 5.

Pharmaceutical Quality Risk Management

This course is covers the key concepts of ICH Q9 and how to apply these to pharmaceutical manufacturing.

Medical Device Quality Risk Management – ISO 14971

This introductory course covers the key concepts of ISO 14971:2007 and how to apply the standard.

Quality Management Systems – ISO 13485:2003

This introductory course covers the basic requirements of ISO 13485 and its implications within a medical device manufacturing company.