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: Events

R Clinic on Clinical Study Design for Medical Devices & Diagnostics

April 27, 2022Events

R Clinic on Clinical Study […]

Read More

Venture Base Camp on Clinical Study Design for Medical Devices and In Vitro Diagnostics

July 3, 2019Events

Venture Base Camp on Clinical […]

Read More

(14 May 2019) – VENTURE BASE CAMP ON ISO 13485:2016 Medical Devices Quality Management – Internal Auditor Training Course – on 28, 29, 30 May 2019

May 14, 2019Events

Venture Base Camp on ISO […]

Read More

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

March 15, 2019Events

  Schedule   Registration   Speakers   Venue […]

Read More

(10 Feb 2019) R-Clinic @PSG-STEP, Coimbatore on 22Feb 2019

February 10, 2019Events

– Date: 22 Feb 2019 […]

Read More

(16 Jan 2019) – VENTURE BASE CAMP ON REGULATORY PROCESSES AND CERTIFICATIONS on 5, 6, 7 Feb 2019

January 16, 2019Events

Venture Base Camp on Regulatory […]

Read More

(15 Nov 2018) Mini-Workshop Series on Regulatory Requirements for Medical Devices – 002 on 08 Dec 2018

November 15, 2018Events

Mini-Workshop Series on Regulatory Requirements […]

Read More

(08 Oct 2018) Mini-Workshop Series on Regulatory Requirements for Medical Devices – 001 on 26 Oct 2018

October 8, 2018Events

Mini-Workshop Series on Regulatory Requirements […]

Read More

(30 July 2018) Report of R-Clinic at Pune held on 28 July 2018

July 30, 2018Events

Report on R Clinic  (R-Clinic-FY1819-02) […]

Read More

(12 July 2018) Report of R-Clinic at Chennai held on 10 July 2018

July 10, 2018Events

Report on R Clinic  (R-Clinic-FY1819-01) […]

Read More

Posts navigation

Older posts
Newer posts
  • 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