Medical Device Regulatory Framework in India
****blogsubmissionsite****/blog/details/medical-device-regulatory-framework-in-india
Medical devices are important products in the healthcare sector. They aid in diagnosing diseases, treating them, and monitoring a patient's health. India has created a strong regulatory framework for medical devices, which guarantees that all medical devices are safe, effective, and of high quality.

#medicaldevice

#registration

#certificate

#healthcare

#license

MD-18 License under CDSCO: Documents, Fees, and Approval Process
****blogosm****/md-18-license-under-cdsco
In India, the importation of medical devices is governed by the Medical Device Rules, 2017, under the regulation of the Central Drugs Standard Control Organization (CDSCO). All foreign manufacturers or India-based importers must secure the MD-18 License as part of their business objectives prior to marketing or selling medical devices in India.
#cdsco
#druglicense
#registration
#certificate

Legal Metrology Packing License for E-commerce & FMCG Businesses in India
https://medium.com/@dsouzaemil....y64/legal-metrology-
In today’s rapidly evolving retail and e-commerce environment, proper labeling and compliance with packaging regulations have become vital components of earning consumer trust. Every product that a retailer or manufacturer sells is subject to compliance with the Legal Metrology (Packaged Commodities) Rules, 2011, as specified by the Legal Metrology Act, 2009.
#legalmetrology
#certificate
#certification
#license

ETA Certificate for Import 2025
https://zekond.com/read-blog/2....63382_eta-certificat
In today’s rapidly evolving electronics market, the ETA Certificate for Import has become a crucial compliance requirement for companies involved in the manufacture, distribution, and sale of wireless and radio frequency (RF) devices.
#wirelessdevices
#certificates
#etacertificate
#import

CDSCO EC Registration Process
https://glasp.co/posts/ded8c62....8-f4fa-4a8a-ace1-e20
The Central Drugs Standard Control Organization (CDSCO) plays a key role in ensuring the ethical and legal compliance of clinical research activities in India. For institutions or organizations conducting clinical trials, CDSCO EC Registration (Ethics Committee Registration) is a mandatory requirement under the New Drugs and Clinical Trials Rules (NDCTR), 2019.
#cdsco
#drugs
#license
#registration
#ethicscommittee