Chetna Dharmavat – Regulatory Information & Facilitation Center

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

April 29, 2022Events

When? – Friday, 29 April […]

Read More

R Clinic on Clinical Study Design for Medical Devices & Diagnostics

April 27, 2022Events

R Clinic on Clinical Study […]

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

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