Clinical Trial
Post-approval changes for medicinal products in the EU
Adriaan Fruijtier
Price:Medical Devices
Medical Devices: EU Directives, Guidance Documents, CE Marking Proc...
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Medical Devices
Masters Certification Program on Annual GLP Refresher
N.S
Price:Medical Devices
Implementing the IMDRF Codes: Essential Adverse Event Reporting Cha...
Kelly Thomas
Price:Medical Devices
Complaint Handling Requirements (US); Interrelationship with CAPA, ...
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Medical Devices
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
Reprocessing Reusable Medical Devices Cleaning & Labeling Requirem...
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Medical Devices
Inspection, Measuring and Test Equipment - A Regulatory Approach
Kelly Thomas
Price:Medical Devices
Meeting Global Unique Device Identification Requirements: Regulatio...
Michael C Redmond
Price:Medical Devices
Medical Device Safety in the Magnetic Resonance Environment CDRHs R...
Kelly Thomas
Price:Medical Devices