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.
The Strategic Shift For most global Cosmetic brands, India’s regulatory journey has begun with import registration — the COS-2 pathway explored throughout this series. But for a growing ..
Regulatory approval is often treated as the finish line. In reality, for Medical Device and IVD manufacturers in India, it marks the start of an equally demanding obligation: Post-Market Surveillance ..
One of the most avoidable and expensive mistakes in Medical Device commercialisation is Regulatory rework — the process of going back to redo documentation, testing, or submissions because the..
India
Global
Sales: +91 7672005050
Reception: +91-11-45214546
9 am to 6 pm (Monday to Friday)