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  2. Food and Drug Administration (Philippines) - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug...

    The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD / ˈ b iː f æ d /; 1982–2009), is a health regulatory agency under the Department of Health created on 1963 by Republic Act No. 3720, amended on 1987 by Executive Order 175 otherwise known as the "Food, Drugs and Devices, and Cosmetics Act", and subsequently reorganized by Republic Act No ...

  3. Validation and verification (medical devices) - Wikipedia

    en.wikipedia.org/wiki/Validation_and...

    The main difference between the two is that validation is focused on ensuring that the device meets the needs and requirements of its intended users and the intended use environment, whereas verification is focused on ensuring that the device meets its specified design requirements. For instance, a regulatory agency (such as CE or FDA) may ...

  4. Philippine Health Insurance Corporation - Wikipedia

    en.wikipedia.org/wiki/Philippine_Health...

    Website. www .philhealth .gov .ph. The Philippine Health Insurance Corporation ( PhilHealth) was created in 1995 to implement universal health coverage in the Philippines. It is a tax-exempt, government-owned and controlled corporation (GOCC) of the Philippines, and is attached to the Department of Health. On August 4, 1969, Republic Act 6111 ...

  5. Napp Pharmaceuticals - Wikipedia

    en.wikipedia.org/wiki/Napp_Pharmaceuticals

    Napp Pharmaceuticals Limited is a private pharmaceutical company in Cambridge, United Kingdom that was founded in 1923 [3] [4] and bought by the Sackler family in 1966. [5] [6] Headquartered together with the related Napp Research Centre in the Cambridge Science Park since the 1980s, [4] it is a sister company of Purdue Pharma and Mundipharma ...

  6. FDA Adverse Event Reporting System - Wikipedia

    en.wikipedia.org/wiki/FDA_Adverse_Event...

    The FDA Adverse Event Reporting System ( FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration 's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses FAERS to monitor for new adverse events and medication errors that might ...

  7. Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug_Administration

    Food and Drug Administration. /  39.03528°N 76.98306°W  / 39.03528; -76.98306. The United States Food and Drug Administration ( FDA or US FDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco ...

  8. Inter-Agency Committee on Anti-Illegal Drugs - Wikipedia

    en.wikipedia.org/wiki/Inter-Agency_Committee_on...

    The Inter-Agency Committee on Anti-Illegal Drugs (ICAD) is an inter-governmental forum in the Philippines responsible for ensuring government agencies in implementing and complying with all policies pertaining to the anti-illegal drug campaign. The agency was formed by Executive Order No. 5, signed by President Rodrigo Duterte on March 6, 2017.

  9. Validation (drug manufacture) - Wikipedia

    en.wikipedia.org/wiki/Validation_(drug_manufacture)

    Validation (drug manufacture) The process of establishing documentary evidence demonstrating that a procedure, process, or activity carried out in testing and then production maintains the desired level of compliance at all stages. In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products ...