Good Manufacturing Practices is the backbone of any and all operations performed in a regulated manufacturing facility. This training is designed to serve as an introductory overview or annual refresher to those already familiar with GMP principles. The content is delivered using an interactive LSM platform and takes on a modular approach based on the Health Canada GUI-0001 and FDA Part 210 & 211 and incorporates quizzes at the end of each of the eight (8) chapters. An electronic certificate will be issued to the learner for their files following successful completion of the training. If you are looking to purchase 10 or more copies, please contact info@psg.ca.

Registration Fee:  

• $435+tax/person 
• $4200+tax/10 people (Group rate)

At some point in the life cycle of a bio-pharmaceutical or medical device product, it will be subjected to a regulated inspection or audit along with that of it’s production facility and personnel. The purpose of this can be to both authorize the manufacturing of the product as well as to ensure that health and safety manufacturing criteria of a product and its production facility are being met. In either case, compliance to all governing regulations must be successfully satisfied in order to receive a passing inspection. The inspection readiness process involves several preparatory steps- all of which have a direct impact on a company’s successful completion of a regulator inspection. This 45-minute, self-paced training is intended to highlight key parts of how to be inspection ready so that you and your company will be prepared for an audit.

Registration Fee:

• $245+tax/person