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CDTM is an expansion of the traditional pharmacist scope of practice, allowing for pharmacist-led management of drug related problems (DRPs) with an emphasis on a collaborative, interdisciplinary approach to pharmacy practice in the healthcare setting. The terms of a CPA are decided by the collaborating pharmacist and physician, though ...
In the United States, the regulation of the pharmacist-to-pharmacy technician ratio is regulated at the individual state level. [1] Some states vary the ratio by institutional (e.g. hospital) pharmacy practice versus retail (i.e. community) pharmacy practice, while others do not regulate pharmacist-to-pharmacy technician ratios at all. [1]
European Union: In the EU, Good Clinical Practice is backed and regulated by formal legislation contained in the Clinical Trial Regulation (Officially Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC). [3]
National Association of Boards of Pharmacy (NABP) is a 501(c)(3) nonprofit organization that assists member boards of pharmacy for the purpose of protecting public health. [3] It has 54 active members and 12 associate members. [6] Active member boards include all 50 United States, the District of Columbia, Guam, Puerto Rico, and the Virgin Islands.
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" stands for the various fields, including the pharmaceutical and food industries, for example good agricultural practice, or GAP.
The Pharmacy and Poisons Act, Cap 244 is an Act of Parliament to make better provision for the Control of the Profession of Pharmacy and trade in drugs and poisons. The Pharmacy and Poisons Board is established as a body corporate, under the Pharmacy and Poisons Act, Cap 244 Laws of Kenya. The PPB is regulatory body within the Ministry of ...
In Portugal, the role of pharmacists in prescribing medications is primarily limited to dispensing, with strict regulations in place. Pharmacists are significantly involved in advising patients on the use of medications, particularly generic drugs, which have become prevalent as a cost-saving measure in the healthcare system.
It appears that electronic prescriptions should be valid [citation needed], especially in the light of the Pharmacy Practice Regulations-2015 declared by the Pharmacy Council of India in January 2015. In these regulations, "prescription," as defined by regulation 2, (j)[3] means "a written or electronic direction from a Registered Medical ...