The Central Drug Standard Control Organization vide notice dated 21 October, 2022 has clarified that anyone who intends to sell, stock, exhibit, offer for sale or distribute a medical device, including in-vitro diagnostic medical devices must obtain the Registration Certificate.
Application for a Registration Certificate must be made with Form MD-41 to the State Licensing Authority (SLA). The registration certificate shall be issued in Form MD-42.
DGFT issued an important public notice updating the policy for the import of Menthol under the Advance Authorization (AA) and Duty-Free Import Authorization (DFIA) schemes
Directorate General of Foreign Trade (DGFT), announced the imposition of a Minimum Import Price (MIP) on Disodium Carbonate (Soda Ash).
Petroleum and Natural Gas Regulatory Board (PNGRB) issued the Petroleum and Natural Gas Regulatory Board (Technical Standards and Specifications including Safety Standards for City or
Government of Karnataka introduced the Karnataka Ground Water (Regulation and Control of Development and Management) (Amendment) Bill, 2024,
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