17BSpuriouscosmetics. SectionsParticulars 17CMisbrandedcosmetics 17DSpuriouscosmetics 18Prohibitionofmanufactureandsaleofcertaindrugsandcosmetics. 18ADisclosureofthenameofthemanufacturer,etc. 18BMaintenanceofrecordsandfurnishingofinformation. 19Pleas. 20GovernmentAnalysts. ...
The government of India in its 72nd year of the republic had drafted the new bill entitled "New Drugs, Medical Devices and Cosmetics Bill 2022" which seeks to replace the existing "Drugs and Cosmetics Act, 1940". Earlier in this Act, Chapter V mentions the support...
The flaws in the 1940 Drugs and Cosmetics Act revealed a poor regulatory framework for medical devices. Hence, the new bill focuses on regulating medical devices as a distinct category. It also acknowledges the role of independent governing authorities with knowledge of medical devices. The objectiv...
"The board recommended that it's necessary to prohibit the manufacture, sale or distribution of these FDCs under Section 26A of the Drugs and Cosmetics Act, 1940, in the larger public interest," it added.
Till date ASU drugs defined under Section 3(a) of the Drugs & Cosmetics Act, 1940 are manufactured for sale under license in accordance with the formulae described in the authoritative books specified in the First Schedule to the Act and are widely consumed by the public due to their traditi...
it means research studies done on people with the aim of evaluating a medical, surgical, or intervention behaviour. 4. cosmetics: under section 3(aaa) of the drugs and cosmetics act, 1940 as, anything which is rubbed, sprinkled or sprayed, and applied to, the human body, beautifying, ...
Clinical Trial Regulations in India: Progress and Challenges Arising from Recent Amendments to Schedule Y of the Drugs and Cosmetics (D&C) Act 1940 (D&C... The Central Drugs Standard Control Organization, which is the drug regulatory authority in India, has recently amended the regulatory framework...
The Drug Controller has directed that appropriate safeguard to the consumers is provided by withdrawing the available stock and take action as per provisions of Drugs and Cosmetics Act 1940 & Rules made there under. The order issued recently by the Drugs Controller to all ...
Relief of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.Nonprescription preparations used for temporary relief of minor skin irritations, itching, and rash caused by eczema, dermatitis, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, ...
It is the “intended use,” as established through product labeling, that can cause the FDA to consider a product to be a drug. The FDA notes that a product can meet the definitions of both cosmetics and drugs, by having two intended uses (such as a shampoo that is also intended to ...