Skip to content
Regulatory Information & Facilitation Center

Regulatory Information & Facilitation Center

— Supporting bio-innovators and entrepreneurs in India —

  • Home
  • About
  • Services
  • Events & Announcements
  • Info Resources
    • COVID19 Collection
  • Contact

R Clinic on Essential Regulatory Requirements for Medical Devices in EU, MDSAP & ISO 13485

By Chetna DharmavatApril 29, 2022Events

When? – Friday, 29 April 2022| Time: 10.30 am – 04.30 pm

Where? –  Venture Center, Pune

Flyer | Outline | 

EUISO 13485MDSAPRegulatory

Post navigation

R Clinic on Clinical Study Design for Medical Devices & Diagnostics
VBC on ISO 13485:2016 Medical Devices QMS & Internal Auditor Training Course
  • Internship Program
    • Exploring EU MDR and its demand in India. Finding out the potential leads for EU MDR 2017/745 services
  • Requirements/preferences
    • Students pursuing B.Pharm / M.Pharm with interest in Regulatory Affairs
    • Basic knowledge of EU MDR and CE marking preferred.
    • Familiarity with market research methods- online surveys, data analysis, and reading industry reports.
    • Familiarity with MS Office tools.
    • Strong communication skills

Click Here To Apply

Copyright © All rights reserved. Theme Meilleur Business by Creativ Themes