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

Category: Uncategorized

Awareness Talk on Understanding of EU MDR 2017/745 (For CE Marking)

October 11, 2023Announcement, Events, Uncategorized

Awareness Talk on Understanding of […]

Read More

Venture Base Camp on : ISO 13485:2016 Medical Devices Quality Management System & Internal Auditor Training Course

March 26, 2022Uncategorized
Read More

Venture Base Camp on : ISO 13485:2016 Medical Devices Quality Management System & Internal Auditor Training Course

February 26, 2022Uncategorized
Read More

eVBC on ISO 13485: 2016 Medical Devices QMS

May 24, 2021Uncategorized

e Venture Base Camp on […]

Read More

eVBC on ISO 13485: 2016 Medical Devices QMS

October 6, 2020Uncategorized

e Venture Base Camp on […]

Read More

e-Regulatory Clinic

July 15, 2020Uncategorized

Regulations, Standards and Certifications for […]

Read More

VBC on ISO 13485: 2016 Medical Devices QMS

August 20, 2019Uncategorized

Venture Base Camp on ISO […]

Read More
  • 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