The Board shall issue guidelines on the refresher program requirement. Repealing Clause.— Republic Act No. 9165, and other applicable laws and issuances; (l) Committing acts in violation of Section 6 of Presidential Decree No. Republic of the PhilippinesCongress of the PhilippinesMetro Manila. 9165 and other applicable laws and issuances. The required information provided by the transferring pharmacy has been recorded. Physician’s Sample.— Pharmaceutical products given or intended to be given free to any health professional by a manufacturer or distributor or its professional service representative as part of its program or promotion shall not be sold to any pharmaceutical outlet or the consuming public. 8981. In refusing the registration, the Board shall give a written statement setting forth the reasons therefor and shall file a copy thereof in its records. b) The pharmacy department shall establish and maintain adequate records of drug purchases necessary for inventory control and legal requirements. In addition, College staff met with major stakeholders from the hospital and community pharmacy sectors, and the Ministry of Health and Long-Term Care to gather feedback on the regulation. Requirements for the Opening and Operation of Retail Pharmaceutical Outlet or Establishment.— The opening of a retail pharmaceutical outlet or establishment shall be subject to requirements provided for in this Act and the rules and regulations prescribed by the FDA. To be appointed a member of the Board of Pharmacy, a person shall be: (a) A natural born citizen of the Philippines; (b) A duly registered pharmacist and has been in the practice of pharmacy for at least ten years; (c) Of good moral character and of recognized standing in the pharmaceutical profession; Hospital Pharmacy: The department of the hospital which deals with procurement, storage, compounding, dispensing, manufacturing, testing, packaging, and distribution of drugs. Section 26. Likewise, a determination regarding an applicant’s approval for licensure cannot … Section 19. Reissuance of Revoked Certificate of Registration, Replacement of Lost or Damaged Certificate of Registration, Professional Identification Card or Special/Temporary Permit.— The Board may, upon petition, reinstate or reissue a revoked COR after the expiration of two (2) years from the date of its revocation. (v) All other acts or omissions analogous to the foregoing. Specifically, the Chief Pharmacist shall: 1. 6675, otherwise known as the “Generics Act of 1988”; (s) Health supplement refers to any product that is used to maintain, enhance and improve the healthy function of the human body and contains one (1) or more or a combination of the following: (1) herbal fatty adds, enzymes, probiotics, and other bioactive substances; and (2) substances derived from natural sources, induding animal, plant, mineral, and botanical materials in the form of extracts, isolates, concentrates, metabolites, synthetic sources of substances mentioned in (1) and (2). Vested Rights; Automatic Registration.— All pharmacists registered before the effectivity of this Act shall automatically be registered hereunder, subject to compliance as to future requirements. Compounding and dispensing shall be done only by duly registered and licensed pharmacists, in accordance with current Good Manufacturing Practice, laboratory practice, Philippine Practice Standards for Pharmacists and dispensing guidelines. The Board shall prepare, adopt, issue, or amend the syllabi or tables of specifications of the subjects in the licensure examination, in consultation with the academe and the Commission on Higher Education (CHED); (d) Recommend the issuance, suspension, revocation, or reinstatement of the COR, PIC or Special/Temporary Permits (STP) for the practice of pharmacy; (e) Administer oaths in accordance with the provisions of this Act; (f) Regulate and monitor the practice of pharmacy in the Philippines, including the practice of subprofessional services such as pharmacy technicians, pharmacy assistants, aides, and other medicine handlers, as described in this Act; adopt measures that may be deemed proper for the enhancement of the profession and the maintenance of high professional, academic, ethical, and technical standards; and conduct ocular inspection of pharmaceutical establishments and higher education institutions (HEIs), in coordination with concerned government agencies; (g) Promulgate and prescribe the Pharmacists’ Code of Ethics, Code of Technical Standards and Guidelines for the Professional Practice of the Pharmacy Profession, in coordination with the APO; (h) Represent the pharmacy profession in all fora involving concerns and issues related to pharmaceutical products and the practice of pharmacy; (i) Investigate cases arising from violations of this Act, the rules and regulations promulgated pursuant thereto, the Pharmacists’ Code of Ethics, Code of Technical Standards and Guidelines for the Professional Practice of the Pharmacy Profession, and other Board issuances; issue summons, subpoena ad testificandum and subpoena duces tecum to secure the attendance of witnesses or production of documents, or both, and other evidence necessary for such investigation or hearing; and render decision thereon which shall, unless appealed to the PRC, become final and executory after fifteen (15) days from receipt of notice of judgment or decision; (j) Delegate the he aring or investigation of administrative cases filed before the Board, except where the issue or question involves the practice of the profession, in which case, the hearing shall be presided over by at least one (1) member of the Board, to be assisted by a Legal or Hearing Officer of the PRC; (k) Conduct, through the Legal Officers of the PRC, summary proceedings on minor violations of this Act, the General Instruction to the Examinees, including the implementing rules and regulations issued by the Board, and to render summary judgment thereon which shall, unless appealed to the PRC, become final and executory after fifteen (15) days from receipt of notice of judgment or decision; (l) Issue and promulgate guidelines on CPD, in coordination with the APO; (m) Recommend the accreditation of the standardized training programs for and certifications of medical representatives or professional service representatives, pharmacy technicians, pharmacy assistants, pharmacy aides and other medicine handlers covered in Section 39, Article IV of this Act. Separability Clause.— If any clause, provision, paragraph or part hereof shall be declared unconstitutional or invalid, such declaration shall not affect, invalidate, or impair the other provisions otherwise valid and effective. Sa paglikha ng alerto sa trabaho na ito, sumasang-ayon ka sa Kasunduan ng Gumagamit , Patakaran sa Pagkapribado , at Patakaran ng Cookie ng LinkedIn.Maaari kang mag-unsubscribe mula sa mga email na ito anumang oras. There are testable success criteria for Section 34. Ratings in the Licensure Examination.— In order to be registered and licensed as a pharmacist, a candidate must obtain a general weighted average of seventy-five percent (75%), with no rating lower than fifty percent (50%) in any of the subjects. An advanced management degree (e.g., M.B.A., M.H.A., or M.S.) NSO / PSA Marriage Contract (for married female applicants) Certified True CopyTranscript of Records with scanned picture and Remarks "For Board Examination Purposes" *Certificate of Internship program duly signed by the dean/program head. The board reviews each incident on a case-by-case basis. Section 50. Compensation and Allowances of the Board.— The Chairperson and members of the Board shall receive compensation and allowances comparable to the compensation and allowances received by the members of the other existing professional regulatory boards under the PRC, as provided for in the General Appropriations Act. BS in Pharmacy. Definition of Terms.— As used in this Act: (a) Accredited professional organization (APO) refers to the duly integrated and accredited professional organization of registered and licensed pharmacists, of which there shall be only one (1), as prescribed under Section 41, Article V of this Act; (b) Adult vaccines refer to cervical cancer, flu (influenza), pneumococcal, other pre-exposure prophylactic vaccines to be administered to patients aged eighteen (18) years and above, and such other vaccines as may be defined by the Department of Health (DOH) in an administrative issuance; (c) Adulterated/Deteriorated pharmaceutical products refer to pharmaceutical products unfit for human consumption, following the standards of quality or purity of which, are as those stated in the United States Pharmacopeia/National Formulary and Philippine Pharmacopeia in its latest edition or any standard reference for drugs and medicines which are given official recognition as well as those provided for in Republic Act No. 5616 on May 23, 2016 and adopted by the Senate as an amendment to Senate Bill No. The PIC shall not be renewed if the requirements for membership with the APO are not met including credit units for attendance to duly accredited CPD. 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