In fulfillment of the requirements of the Drugs and Cosmetics Act of 1940, the IPC is publishing an official book of standards for drugs known as the Indian Pharmacopoeia (IP). There are 44 ophthalmic active pharmaceutical ingredients (APIs) and combinations approved by CDSCO as of 201 I; the...
The field of nanomedicine has significantly influenced research areas such as drug delivery, diagnostics, theranostics, and regenerative medicine; however, the further development of this field will face significant challenges at the regulatory level if related guidance remains unclear and unconsolidated. Th...
common way of taking medicine is oral ingestion for internal use but in some ailments, topical application is frequently employed in the form of paste. Decoction of the leaves is administered for dyspepsia, jaundice, and cardiac and respiratory problems and is used as a tonic [82]. The major ...
Indian PharmacopoeiaPRSharmonizationherbal drug standardsreference substancesThe benefits of herbal drugs were well understood way back. They have been used for the promotion of health and medical purposes - in disease conditions. It is a conventional belief that herbal drugs have no side effects, ...
Therapeutic Innovation & Regulatory ScienceKlaiselvan V, Prakash J, Muthusamy K, Singh GN. Quality stan- dards and current status of ophthalmic formulations in Indian Pharmacopoeia and National Formulary of India. Ther Innov Reg- ulat Sci. 2014;48(3):386-392....
Regarding the evaluation of food safety in Europe, the European Food Safety Authority (EFSA) regulates the standards for food and are updated on a regular basis. Whereas, the European Pharmacopoeia provides defined guidelines that specify maximum permissible amounts of live microorganisms for ...
Illicium verum Hook. f. is a globally significant spice, which is recognized in China as a food-medicine homolog and extensively utilized across the pharmaceutical, food, and spice industries. China boasts the world’s leading resources of I. verum, yet
A requirement has recently been set by the European Pharmacopoeia and the U.S. Food and Drug Administration for the uniformity of mass of subdivided tablets. For breaking ease, an in-vivo reference test and a routinely applicable in-vitro test need to be established. Keywords: pharmaceutics; ...