The Central Drugs Standard Control Organization through notice dated 23 August, 2021 has Classified Medical Devices Pertaining to Pediatrics and Neonatology. The list of devices classified into risk category A,B and C is enlisted in the notice and their intended use is provided. Only the general intended use is provided and other uses shall be specified by manufacturer. The list will be revised from time to time.
FSSAI Empowers Consumers to Report Misleading Food Claims via App and Portal
The digital tool simplifies the submission of crucial details necessary for regulatory action. Consumers can now easily upload front-of-pack images clearly highlighting the misleading claim,