CDSCO Medical Device Registration and Regulatory Approval Process in India
by Mahek Sancheti on 2024-09-18
The Indian growing healthcare market opens a large number of opportunities in the world for medical device companies.
Maximizing Sustainability and ESG Impact
by Mahek Sancheti on 2024-09-18
In a world where environmental concerns, social responsibility, and governance issues are at the core of global conversations, it is not optional but imperative to have maximum sustainability and ESG impact.
The Scope of Drug Manufacturing Licenses in Uttar Pradesh
by Tanya Sharma on 2024-09-17
In India, the pharmaceutical industry plays a pivotal role in providing essential medicines and contributing to public health. Drug manufacturing is a highly regulated sector, requiring adherence to stringent quality standards and legal requirements.
BIS Registration: Apply for BIS license Online in India
by Parul Bohral on 2024-09-17
BIS registration is Bureau of Indian Standard, BIS, carries out a certification process. This registration is essential to ensure specific quality and safety requirements before they are sold in the Indian markets.
What is RoHS? Why RoHS Compliance Testing is important?
by Mahek Sancheti on 2024-09-17
The current global market integrates electronics and electrical equipment into part of life, and they touch very many areas. These devices, ranging from smartphones and laptops to household gadgets and industrial appliances, are not only full of mighty capabilities..
Non-Notified Medical Devices Registration and Approval in India
by Tanya Sharma on 2024-09-13
The Indian medical device industry is growing rapidly, driven by continuous technological advancement, increasing healthcare needs, and a rising emphasis on improvement in patient outcomes. Much complexity is involved in navigating the regulatory landscape of non-notified medical devices.