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The Certified Medical Device Compliance Professional (CMDCP) program gives you the compliance training needed to advance your career and satisfy regulatory training requirements.
- Certification Programs
We offer on-site pharmaceutical training and life science...
- Certification Programs
The Dual Certificate Program in medical devices and pharmaceuticals. has the most comprehensive curriculum and includes eight electives you hand pick from dozens of options, spanning the topical areas of clinical, quality, pharmaceuticals and biologics, medical devices, and regulatory essentials.
Learn the requirements for CE marking under the MDR 2017/745. Discover our MDR dedicated training portfolio developed to help you navigate the requirements, implementation, and conformance.
Identify the pre-market regulations and pathways to market for medical devices in the United States. Distinguish how the Food and Drug Administration (FDA) classifies medical devices. Recognize when clinical data is required and the basic requirements for conducting clinical investigations.
The Regulatory Affairs Certificate: Medical Devices provides a cost-effective, convenient option that will equip you or your organizational team with the tools and knowledge needed to progress as a regulatory professional and stay ahead of the competition.
We offer on-site pharmaceutical training and life science certification programs for organizations with 10 or more employees enrolling. Contact a Training Advisor to learn more. View all courses
Medical device manufacturers need to maintain compliance, ensure patient safety, and navigate risk-related requirements effectively. Our training covers all aspects of MDR, including labeling and UDI requirements.
