FDA: Software Assurance guidance for Production and Quality System Software Written by admin on February 20, 2024. Posted in Regulations.
Language requirements for Manufacturers – Europe Written by admin on February 13, 2024. Posted in Regulatory Information Management.
Mexico: Modifications to Medical Device Registration Written by admin on November 8, 2023. Posted in Regulations.
Is Regulatory Team Overworking but Unproductive? Written by admin on November 7, 2023. Posted in Regulatory Automation.
Swissmedic Device/IVD Database Key Dates Written by admin on November 6, 2023. Posted in Regulations.
