Medical Devices
Medical Devices: EU Directives, CE marking, ISO Certification and t...
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Medical Devices
Writing and Revising SOPs for Increased Operational Efficiency
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Medical Devices
Creation Of Dhfs, Dmrs, and Dhrs Utilizing The Principles Of Lean D...
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Medical Devices
6 Hrs Virtual Seminar-Investigational New Drug (IND) & Investigatio...
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Clinical Trial
Post-approval changes for medicinal products in the EU
Adriaan Fruijtier
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Medical Devices: EU Directives, Guidance Documents, CE Marking Proc...
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Medical Devices
Implementing the IMDRF Codes: Essential Adverse Event Reporting Cha...
Kelly Thomas
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Post Market Surveillance with the new Medical Device Regulation EU ...
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Medical Devices
Risk-Based Supplier Control: How to Meet FDA and Your Iso 13485 Not...
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Medical Devices
Inspection, Measuring and Test Equipment - A Regulatory Approach
Kelly Thomas
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