Medical Device Labeling

Medical Device, Drugs, API’s, Food products exported from one country to other requires compiling with the labeling requirements of the importing country in addition to the requirements of the country of origin.

The products marketed in the United States, European region ether they are manufactured here or are imported from abroad, must comply with the labeling requirements, if the labeling of a is not comply with regulations or requirements it will be considered as misbranded. A "label" is a display of written, printed or graphic matter upon the immediate container of any article.

"Labeling" includes all labels and other written, printed or graphic matter upon any article or any of its containers or wrappers, or accompanying such article.

The labeling standards accepted by the Europe are EN 980 whereas US follows FDA regulations.

AVSCS can help Medical Device, Pharmaceuticals, Food, Cosmetic, and Nutraceuticals companies to review and modify your labeling to comply with respective country regulations. ​

Contact us

A1-101, Ankur,
Near Cipla Foundation,
Warje, Pune- 411058

E mail :-
Telephone :- +91 - 9881946595

Design & Developed By : Logic Palace Systems and Softwares
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