Program Announcement

ISO 13485:2016 – Lead Auditor Training (Medical Device Quality Management Systems ) Indian Biomedical Skill Consortium (IBSC) is Conducting Lead Auditor Training program on ISO 13485:2016 Standard (Medical Device Quality Management Systems ) at Kalam Convention Center, AMTZ Campus, Vizag.… 

CDSCO Notification

Regulation of all Class A & B Medical Devices under Licensing regime, w.e.f 01.10.2022 – Regulator’s Notification MoHFW has released a recent notification on Sep 30th 2022 about the Registration / Licensing norms for Medical Device Manufacturers, Importers for Class… 

Webinar on Medical Devices

Webinar on Regulations for Medical Devices AIMED (Association of Indian Medical Device Industry) is organising a webinar session for the benefit of MSME Manufacturers in the Medical Device Manufacturing space , to guide them about the Registration Process to be completed… 

Medical Devices Rules 2017 (MDR-17) – Regulation of Medical Devices

Medical Devices Rules 2017 (MDR-17) – Regulation of Medical Devices Challenges of Regulation in Medical Devices Chandigarh Chapter, PHDCCI is organizing Interactive Video Conference on Medical Devices Rules 2017 (MDR-17) – Regulation of Medical Devices | Challenges of Regulation in… 

Indian Medical Device Sector

Role and Scope of ICMED Certification Schemes ICMED Certification Schemes launched by Quality Council of India jointly with Domestic Manufacturers Industry Association in India, is purely a Voluntary Certification Program . Medical Buyer Magazine has covered an interesting article by…