CDSCO (India)
NOTICE
Draft Guidance document for Manufacturers of In-vitro diagnostic Medical device for stakeholders comment
Published: 10/9/2026Detected: 10/9/2026
Summary preview
Draft guidance for stakeholders on India CDSCO regulatory expectations for manufacturers of in-vitro diagnostic (IVD) medical devices, intended to solicit industry comments before finalization.
Get the full analysis, free
Create a free account to see the complete summary, key takeaways, and why this matters for your products, and to get alerts like this by email.
Create free accountmanufacturing
quality
clinical
safety
labeling
#India CDSCO
#in vitro diagnostic
#IVD medical device
#stakeholder consultation
#regulatory submission
Official Source Document Source Verified
Access the original document directly from INDIA CDSCO.
More from CDSCO (India)
- Surrender of Cosmetic Registration Certificate No. RC/COS-005067 dated 05.07.202410/6/2026
- 2026.09.28 G.S.R. 861(E)_Draft proposal for Change in conditions of Retail and Wholesale license w.r.t. advertisement.9/28/2026
- Indiscriminate use of painkillers (NSAIDs), antibiotics and associated risk of Chronic Kidney Disease9/22/2026
- LIST OF REGISTRED BA-BE STUDY CENTRE & BIO-ANALYTICAL LABORATORY under NDCT Rules 20199/18/2026
- Public Health alert against the use of unauthorised Cosmetics Products9/14/2026