This is a fast-moving, intensive training course aimed at Managers, Supervisors and Technical Staff working in the pharmaceutical industry.
As well as establishing the key requirements of GMP, the course focuses on the application of GMP in the working environment.
With recently announced changes in the regulatory approach to GMP compliance, delegates will be introduced to a number of science-base risk management tools, techniques and methodologies.
- Introduction to GMP
- Managing Quality
- Regulatory Approach to Risk Management – current and future trends
- Documentation and Records
- Contamination Control
- Manufacturing and Packaging GMPs
- PAT & Process Control
- Internal and External Audit Programmes
The course consists of a lively mix of presentations, group exercises and discussions. At the end of the course, there will be a short quiz to test understanding. Copies (pdf) of all presentation slides and handouts will be provided.
A complimentary information pack containing course details and preparatory exercises will be sent to each delegate prior to the start of the course.
Out of Class Assignment
Delegates are offered the opportunity to complete a GMP assignment following completion of the course. This will be facilitated and supported remotely by SeerPharma’s team of consultants and successful completion will be rewarded with additional certification. There is no additional charge for this.
Next Course Date : 20th – 22nd November 2017
Venue : Copenhagen, Denmark
Course fee : €2,395
If you would like further information on this course please call us on +44 (0)1903 730622 or e-mail email@example.com