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An excipient is a substance formulated alongside the active ingredient of a medication.They may be used to enhance the active ingredient’s therapeutic properties; to facilitate drug absorption; to reduce viscosity; to enhance solubility; to improve long-term stabilization (preventing denaturation and aggregation during the expected shelf life); or to add bulk to solid formulations that have ...
These courses focus on specialty areas of healthcare-related issues and are intended to provide pharmacy students, pharmacists, medical doctors, nurses, and other healthcare professionals with applicable knowledge that can be used in a variety of work environments such as retail pharmacies, hospitals, or poison control centers.
International Pharmaceutical Excipients Council is a global organization founded in 1991 representing producers, suppliers, and end users of excipients. The body has three divisions in Europe , Japan , and the United States , each of which focuses on local regulations concerning the excipients market, as well as on new research and business ...
The institute offers Masters and Doctoral degrees in pharmaceutical sciences. As an Institute of National Importance, it plays a major role in human resource development for the Indian pharmaceutical industry. [1] [2] The institute is located at the former R&D Center of IDPL, Bala Nagar and Hyderabad. [3]
Drug Master File (DMF) is a document containing complete information on an Active Pharmaceutical Ingredient (API) or finished drug dosage form.It is known as European Drug Master File (EDMF) or Active Substance Master File (ASMF) and US-Drug Master file (US-DMF) in Europe and United States respectively.
The courses that grant an academic degree are accredited by the Agency for Assessment and Accreditation of Higher Education (A3ES) [2] and the Integrated Master in Pharmaceutical Sciences is also accredited by the Portuguese Pharmaceutical Society (Ordem dos Farmacêuticos) for professional practice. [3]
The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country; [1] it is often mentioned in conjunction with the electronic Common Technical Document (eCTD).
The dosage form for a pharmaceutical contains the active pharmaceutical ingredient, which is the drug substance itself, and excipients, which are the ingredients of the tablet, or the liquid in which the active agent is suspended, or other material that is pharmaceutically inert. Drugs are chosen primarily for their active ingredients.
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