C. §2500 through §2551) • Board of Pharmacy Rules and Regulations • Delaware Code. Answer: Section 11.6 of the Board’s Rules and Regulations delineates the duties and responsibilities of a consultant pharmacist and provider pharmacy. Pharmacist-in-Charge Self-Inspection Report: • within 30 days of your first being designated as PIC, and • by February 1 of each year while you continue as the PIC. Laws, c. 378, § 2; 68 Del. All. h. Administration of injectable medications, biologicals and adult immunizations pursuant to a valid prescription or physician-approved protocol approved by a physician duly licensed in the State under subchapter III of Chapter 17 of this title. The Ontario College of Pharmacists is the registering and regulating body for the profession of pharmacy in Ontario. (6) “Distant site” means a site at which a health-care provider legally allowed to practice in the State is located while providing health-care services by means of telemedicine or telehealth. The secondary objective of the Board is to maintain minimum standards of professional competency in the practice of pharmacy. Laws. (c) The Executive Secretary, who is an ex officio member of the Board without a vote, is responsible for the performance of the regular administrative functions of the Board and other duties as the Board may direct. The person requesting a transcript incurs the expense of preparing the transcript. Laws, c. 167, § 1; 79 Del. Laws, c. 206, § 1; 72 Del. Laws, c. 238, § 1; 80 Del. (1) “Biological product” means a biological product as defined in § 351 of the Public Health Service Act (42 U.S.C. (20) “Pharmacist” or “licensee” means an individual licensed by the State pursuant to this chapter to engage in the practice of pharmacy. A copy of such inventory will be sent to the Office of Controlled Substances and another copy retained on the premises. Do I need to reapply for a new license if there is a controlling interest change in ownership of a pharmacy? Please read the important COVID-19 information from the Division of Professional Regulation More Info. Retain another copy on the premises for a period of at least two years. For a complete copy of the Delaware Medical Marijuana Act, contact the DPH Office of Medical Marijuana, or With the renewal deadline approaching, the Delaware State Board of Pharmacy and the Delaware Division of Profes - sional Regulation would like to ensure that all pharmacists understand their continuing education (CE) requirements. The e-mail will provide a link to the Newsletter. Tax Center Section 188.8.131.52 of the Board’s . Delaware Courts Laws, c. 159, § 1; 74 Del. Elected Officials § 262. d. A substance intended for use as a component of any substance specified in paragraph (8)a., b. or c. of this section. A person who has been twice appointed to the Board or who has served on the Board for 6 years within any 9-year period may not again be appointed to the Board until an interim period of at least 1 term has expired since the person last served. 68 Del. Pure Drug Regulations; Section 2500-7.0 - Non-pharmacy Outlets Handling Legend Veterinary Drugs; Section 2500-8.0 - Requirements for Obtaining a Permit as a Wholesaler, Manufacturer, Outsourcing Facility or Third-Party Logistics Provider ; Section 2500-9.0 - … Records kept in accord with this section are prima facie evidence of the proceedings of the Board. When the FDA has rated a branded drug with an AB rating, you may substitute the generic for the branded drug. Prescriptions o §4740. The consultant pharmacist must notify the Board in writing within ten days of starting as a consultant in Delaware. The Office of Controlled Substance (OCS) recommends that the incoming and outgoing PICs take the inventory at the same time, either at the start or the close of the business day. 1.1. (4) “Direct supervision” means oversight and control by a licensed pharmacist who remains on the premises and is responsible for the work performed by a subordinate. State Agencies b. Whenever the pharmacist in charge of a pharmacy in the State of Delaware leaves his position, a complete inventory of all medication covered by 16 Del.C. Laws, c. 206, § 1; 70 Del. Laws, c. 412, § 1; 74 Del. The reasoning behind this rule is that a medication that has left the control of the pharmacy is susceptible to any range of issues that could affect its safety and effectiveness in treatment. date and time that the inventory was completed. Laws, c. 167, § 1; 77 Del. Answer: FDA approval for any drug product addresses quality concerns for the manufacturing process of that particular medication. Whether a product can be used as a generic equivalent of a brand name product depends on the rating of the branded product. (28) “Reference product” means a product as defined by the Federal Food and Drug Administration pursuant to 42 U.S.C. The Delaware State Board of Pharmacy News is published by the Delaware State Board of Pharmacy and the National Association of Boards of Pharmacy Foundation, Inc, to promote compliance of pharmacy and drug law. Laws, c. 95, § 3; 24 Del. Laws, c. 141, §§ 1, 2; Code 1915, §§ 858, 861, 868, 875; 28 Del. Section 1.5 explains CE programs. mandates Laws, c. 238, § 1; 80 Del. An area partitioned by a five-foot divider on two sides with a minimum of nine square feet would satisfy this requirement in most settings. The boards/commissions also maintain standards of professional competence and service delivery. (10) “Executive Secretary” means the executive secretary of the Delaware State Board of Pharmacy who shall be a pharmacist. What are the building requirements for a new pharmacy located in Delaware? Laws, c. 262, § 42; 76 Del. Laws, c. 206, § 1; 70 Del. (30) “Store and forward transfer” means the transmission of a patient’s medical information either to or from an originating site or to or from the provider at the distant site, but does not require the patient being present nor must it be in real time. (a) The Board shall hold regularly scheduled business meetings at least 6 times in a calendar year, and at other times as the President of the Board considers necessary, and at the request of a majority of the Board members. How do I log into RELIAS to complete my CNA CEUs? (h) The provisions of the State Employees’, Officers’ and Officials’ Code of Conduct set forth in Chapter 58 of Title 29 apply to the members of the Board. If the CE provider is neither an approved American Council on Pharmaceutical Education (ACPE) provider nor Board-approved provider, you may submit a Service Request for CE Provider ApprovalÂ in DELPROS online portal for CE approval. The opinions and views expressed in this publication do not necessarily reflect the official views, opinions, or policies of the Foundation or the Board unless expressly so stated. Laws, c. 140, §§ 7, 10; Code 1915, §§ 856, 859; 36 Del. Pharmacy license number, Controlled Substance registration number and Drug Enforcement Administration registration number, name of the PIC responsible for the closing. Del. (k) The Pharmacy Regulatory Council shall fall under the authority of the Board of Medical Licensure and Discipline and shall consist of 4 pharmacists and 1 member of the public appointed by the Board of Pharmacy, and 2 physicians appointed by the Board of Medical Licensure and Discipline. It also licenses pharmacies (both in Delaware and elsewhere), pharmaceutical manufacturers and distributors, medical gas dispensers and retail businesses that sell non-controlled prescription drugs for veterinary use. Related Topics: Board of Pharmacy, Department of State, Division of Professional Regulation, DPR, frequently asked questions, State of Delaware, Delaware's Governor The inventoryÂ must include: Is a Pharmacy or Pharmacist allowed to accept returned medications for re-dispensing? (17) “Originating site” means a site in Delaware or outside of Delaware if the patient is a Delaware resident at which a patient is located at the time health-care services are provided to him or her by means of telemedicine or telehealth, unless the term is otherwise defined with respect to the provision in which it is used; provided, however, notwithstanding any other provision of law, insurers and providers may agree to alternative siting arrangements deemed appropriate by the parties. Answer: Pharmacy applications (whether new, relocated or remodeled) must be accompanied by three copies of floor plans, drawn to scale, of the proposed prescription department. A person who is subpoenaed may be required to testify in any and all matters within the jurisdiction of the Board. (7) “Division” means the Division of Professional Regulation. 68 Del. The Call Center will open Friday, Dec. 18, and will be operational from 8:30 a.m. to 4:30 p.m., Monday through Friday, and from 10:00 a.m. to 4:00 p.m., Saturday. What are my responsibilities as a Pharmacist-In-Charge? Division of Professional Regulation. A person who is a member of the Board on July 24, 2007, may complete that person’s own term. Business First Steps, Phone Directory The primary objective of the Board of Pharmacy is to promote, preserve, and protect the public health, safety, and welfare. C. Â§ 2549 (c) on prescription forms. This includes, but is not limited to, labeling requirements in 24 Del. Rules and Regulations describes this requirement. The sections of Delaware law that explain your duties are . Please read and follow instructions carefully. The counter must contain an additional space for computers if applicable. To meet these objectives, each board/commission 1. develops standards for professional competency 2. promulgates rules and regulations 3. adjudicates complaints and, when necessary, imposes disciplinar… Do not create or register an account for yourself in … Delaware Board of Pharmacy – These materials are available online at . name, address and phone number of the licensed pharmacy to which prescription drugs, prescription files and patient profiles will be transferred. 47 be taken by the present and prospective pharmacist-in-charge. These requirements apply to all applications, whether initial filing or re- application. (29) “State” means the State of Delaware. C., Chapter 25. Pharmacy Rules; Rule 17 Appendix A; Rule 17 Appendix B; Rule 17 Appendix C Const. 24 Del. DOVER, DE – All Delaware prescribers and pharmacists can now integrate their electronic health record and pharmacy management systems with the state’s prescription monitoring program (PMP), the Delaware Division of Professional Regulation has announced. C. 1953, §§ 2503, 2506, 2507, 2509; 53 Del. If you are unable to reach us by phone, submit your inquiry via email at firstname.lastname@example.org.Please read the important COVID-19 information from the Division of Professional Regulation More Info Effective 10/22/2020 a Security Code is no longer required for registration. 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