The medical device and pharmaceutical quality industry is constantly changing, as evidenced by recent quality and regulatory updates. Revisions to ISO 9001 and ISO 13485, major changes associated with MDSAP and EU MDR, and new expectations in some areas for additive manufacturing have made staying on top of what’s going on in our ever-changing industry harder than ever. As technology and markets evolve, regulations are racing to stay ahead of the curve, putting a great burden on quality professionals to keep pace.
While there many options available to help you keep pace with new requirements, Medpoint has a team of consultants with proven training and real-world expertise. Our Medpoint University training program can be tailored to fit your specific need, whether it be a small group training part of a larger company wide training to revised standards.
Medpoint University instructors have the credentials to provide quality training and are available to come onsite or perform training remotely. Using a broad base of practical experience and an ability to connect with their audience, our trainers craft presentations and exercises that ensure you get the most from each training session.
Some recent examples of training conducted through Medpoint University are: Overview of updates to ISO 13485: 2016 and ISO 9001: 2015, MDSAP expectations awareness, and Lead Auditor/Internal Auditor Training.
Whatever your specific need, Medpoint has the experts available to provide proven, quality training uniquely tailored for your specific needs. To learn more, contact us at firstname.lastname@example.org or 800.200.9292.