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Medical Devices
August 30, 2024
August 30, 2024
Ensuring Regulatory Compliance: Managing Global and Local Literature Surveillance for Drugs and Medical Devices for a Leading Pharmaceutical Company
Managing Global and Local Literature Surveillance: Case Study Overview Client
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February 19, 2024
February 19, 2024
GAP analysis and CER assessment for CE certification: A simple path to EU-MDR compliance
April 26, 2021
April 26, 2021
US Medical Device Regulations
Key Regulations & Guidelines: Medical Device Reporting – 21 CFR
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April 26, 2021
April 26, 2021
EU Medical Device Regulations
April 26, 2021
April 26, 2021
Post-Brexit Medical Device Regulations
April 26, 2021
April 26, 2021
Safety & Regulatory requirements for Medical Devices
April 26, 2021
April 26, 2021
Technological Advancements in Medical Devices
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