The items which are not restricted can be easily imported but, the ones which are restricted need to get approval from DGFT (Directorate General of Foreign Trade). We at CliniExperts provide consultation and assistance to our clients regarding the import of restricted items in India. We provide the following services:
Not only at DGFT, have we helped our clients in liaisoning process at Central Insecticides Board and registration committee, Faridabad.
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)