The Islamic Republic of Afghanistan has officially acknowledged the Indian Pharmacopoeia (IP), a well-known drug standards book. The text will now be utilized in Afghanistan to maintain health product quality.
Understanding the Indian Pharmacopoeia
The Indian Pharmacopoeia is an officially recognized source of drug standards as specified by the Drugs and Cosmetics Act, 1940, and Rules 1945. Under the Second Schedule of this Act, the IP is established as the official guideline for drugs being imported, manufactured for sale, stocked, or exhibited for sale or distribution in India.
This standard-setting publication defines the identity, purity, and strength of drugs produced and marketed in India. It is considered an authoritative resource, and its regulations are enforced by Indian regulatory authorities to control medicine quality.
The IP is regularly updated by the Indian Pharmacopoeia Commission to improve drug quality, with new additions and updates to existing monographs forming part of an official document.
The Role of the Indian Pharmacopoeia Commission
The Indian Pharmacopoeia Commission is an independent entity under the Ministry of Health and Family Welfare responsible for setting drug standards in India. Its main goal is to enhance public and animal health by establishing authoritative and officially accepted standards for drug quality, including active pharmaceutical ingredients, excipients, and dosage forms.
These standards are used by health professionals, patients, and consumers alike. In addition, the Commission develops IP Reference Substances (IPRS), which serve as identification markers for the substance under test and its designated purity as detailed in the IP monographs.
| Fact | Description |
|---|---|
| Formal Recognition | The Islamic Republic of Afghanistan has formally recognized the Indian Pharmacopoeia (IP) |
| Role of IP | IP is an official resource of drug standards as per the Drugs and Cosmetics Act, 1940, and Rules 1945 |
| Administration | The Indian Pharmacopoeia Commission, under the Ministry of Health and Family Welfare, is responsible for setting drug standards in the country |
The Drugs and Cosmetics Act, 1940
The Drugs and Cosmetics Act, 1940, is a legislative act that regulates the import, manufacturing, and distribution of drugs in India. Its primary objective is to ensure that the drugs and cosmetics sold in India are safe, effective, and comply with safety standards and parameters.