On-Site Regulatory and Quality Management Training Courses
Our quality assurance and regulatory training classes are conducted by QA and RA professionals with many years of medical device manufacturing experience. All of our training is conducted at your facility and tailored to your needs. Because we charge a fixed fee regardless of the number of attendees, Emergo QA and RA training is a great value if you are training more than two people. Your team will get the highest quality training available from people who understand the real world application of what they are presenting. Training classes are available on the following topics. All classes are conducted in English.
- FDA Good Manufacturing Practice (GMP) training
- ISO 13485:2003 overview training
- ISO 14971:2007 overview training
- CE Marking training
- Integrating GMP/ISO 13485/CE Marking & Canadian Medical Device Regulations
- FDA GMP & ISO 13485 internal auditor training
Speaking engagements
If you are a meeting planner looking for speakers at your upcoming event, please contact us. We have given presentations at numerous trade shows, association seminars, corporations and other organizations on topics including:
- CE Marking for medical devices.
- Quality assurance as it relates to ISO 13485 or ISO 9001.
- Medical device regulations in Europe, USA, Australia and Canada.
- Post market surveillance of medical devices.
- European packaging waste regulations.
- Finding and selecting distributors for your product(s) in Europe or the USA.
- And many other quality and regulatory topics.
