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September 11, 2024
September 11, 2024
Successfully Enabled CTD Modules Preparation within Stringent Timelines
Submission of Common Technical Document Modules: Case Study Overview A
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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
March 7, 2023
March 7, 2023
PSUSA procedures and implementation of the outcome of a PSUSA procedure
August 8, 2022
August 8, 2022
Designing a Safety and Risk Management System for Cellular Therapies
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