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

International Workshop on MedTech Products – Navigating Global markets & regulations 25-26 March 2019, New Delhi (India)

By Chetna DharmavatMarch 15, 2019Events

 

Schedule   Registration   Speakers   Venue

 

Post navigation

(10 Feb 2019) R-Clinic @PSG-STEP, Coimbatore on 22Feb 2019
(14 May 2019) – VENTURE BASE CAMP ON ISO 13485:2016 Medical Devices Quality Management – Internal Auditor Training Course – on 28, 29, 30 May 2019
  • 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