Startup Launch Acceleration Program | […]
Awareness Talk on Understanding of EU MDR 2017/745 (For CE Marking)
Awareness Talk on Understanding of […]
R Clinic on Planning Regulatory Pathway & Essential Requirements for Medical Devices & IVDs for the Indian Market
R Clinic on Planning Regulatory […]
R Clinic on Understanding documentation requirements for EU MDR 2017/745
R Clinic on Understanding documentation […]
Mentor Mixer on Understanding of EU MDR 2017/745 for European Approval
Mentor Mixer on Understanding of […]
R Clinic on Understanding documentation requirements under EU MDR 2017/745
R Clinic on Understanding documentation […]
R Clinic on Designing Clinical Trials for Medical Devices & Biopharmaceutical Products
R Clinic on Designing Clinical […]
R Clinic on Planning Regulatory Pathway & Essential Requirements for Medical Devices & IVDs
R Clinic on Planning Regulatory […]
VBC on ISO 13485:2016 Medical Devices QMS & Internal Auditor Training Course
Venture Base Camp on ISO […]
VBC on Requirements of the Medical Device Regulation (MDR) for CE marking
Venture Base Camp on Requirements […]