The Indian healthcare industry is one of the world’s largest healthcare setup. Being the 2nd largest population in the world, the healthcare of this burgeoning people is funded by either healthcare insurance, government, employer but largely by the patient themselves. With increasing interest by the Indian Government to organize and improve the healthcare sector, patient interest, local business interest and international collaboration are all at the forefront. With this in mind, an Indo-German medical device conclave was held in New Delhi, by a collaboration between CliniExperts and the Federal Ministry for Economic Affairs and Energy, Germany.
Read the full case study here –
Saurangi is a food regulatory expert with 8 years of experience. She shares her knowledge and insights on regulatory updates, food trends, best practices, and news. Follow her for expert insights and practical advice on all things for food regulatory
CliniExperts Services Pvt. Ltd.
Summary Short Description Strict regulatory protocols govern clinical investigations for medical devices. Central to this process are forms MD-22 and MD-23. Form MD-22 is an application to Central Lic..
Navigating Software as a Medical Device regulation involves addressing varying global standards, including risk-based classifications...
The future of Software as a Medical Device will see breakthroughs in Artificial Intelligence-based diagnostics, personalised treatments, and remote monitoring...
New Delhi
Unit No. 324 & 325, City Centre Mall, Plot No. 5, Sector 12, Dwarka, India - 110075
+917672005050
Bengaluru
RMZ Galleria, 1st floor, Ambedkar Colony, Yelahanka, Bengaluru, Karnataka, India – 560064
Sales: +91 7672005050
Reception: +91-11-45214546
9 am to 6 pm (Monday to Friday)