Medical Devices and IVDs Training
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Featured Medical Devices Training
MDSAP Overview and Country-Specific Medical Device Regulations: 5-Course Bundle
CQI/IRCA-certified QMS Lead Auditor based on ISO 13485:2016 and MDSAP Requirements
September 19 – 23, 2022
ISO 14971:2019 Risk Management for Medical Devices and IVDs-Practical Application
October 26 – 27, 2022
Key FDA Policies, Procedures and Practices Before, During and After Medical Device Manufacturer Inspections
Two of the Most Common IVDR Challenges (With Solutions)
Insights and Expertise
White Paper: Tools and Tips for Writing Effective Nonconformity Statements During Quality Management System Audits of Medical Device Manufacturers