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

Mini-Workshop Series on

Regulatory Requirements for Medical Devices

HOW TO WRITE A QUALITY MANUAL?

Good Documentation Practices, SOPs, and Quality Manual

When? – Saturday, 08 Dec 2018 | Time 1345-1830 Hrs

Where? – E – Class Room, Venture Center, 100 NCL Innovation Park

Queries? – Lipika Biswas |020-25865875/76/77|eventsdesk@venturecenter.co.in

Flyer |  Workshop Outline | Workshop Feedback

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

Mini-Workshop Series on

Regulatory Requirements for Medical Devices

How to become an ISO 13485 Certified Medical Devices Company?

Topic: Introduction to ISO 13485 and QMS Implementation Strategy

When? – Friday, 26 Oct 2018 | Time 1345-1730 Hrs

Where? – Lecture Theatre, Venture Center, 100 NCL Innovation Park

Flyer |  Workshop Outline | Workshop Feedback 

(7 July 2018) Advisory service launched

RIFC is pleased to announce the launch of its first advisory service. RIFC shall start with a basic advisory service to guide entrepreneurs. In the coming months, many more services will be launched. RIFC aims to inform and facilitate regulatory approvals for bio-entrepreneurs. It will work closely with experience entrepreneurs, experts, consultants and regulators to achieve this goal.

More details on services: http://rifc.venturecenter.co.in/services/

(9 June 2018) RIFC website launched

The RIFC website has been launched. The future plan is as follows:

  • July 2018:  RIFC core staff in place. Launch of first service offering. “The Regulatory Collection” in the Venture Center Library to be launched.
  • August 2018:  The RIFC Wiki (Ver 1) to be launched. First RIFC event to be launched.