Medical Devices

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
February 19, 2024
medical Information Systems

GAP analysis and CER assessment for CE certification: A simple path to EU-MDR compliance

April 26, 2021

US Medical Device Regulations

Key Regulations & Guidelines: Medical Device Reporting – 21 CFR
April 26, 2021

EU Medical Device Regulations

April 26, 2021

Post-Brexit Medical Device Regulations

April 26, 2021

Safety & Regulatory requirements for Medical Devices

April 26, 2021

Technological Advancements in Medical Devices