https://dpr.delaware.gov/ and click . Public Meetings § 501(c)(3)) to a nonprofit affiliate of the charitable organization to the extent permitted by law; 2. (f) The Governor shall suspend or remove a member of the Board for the member’s misfeasance, nonfeasance, malfeasance, misconduct, incompetency, or neglect of duty. (3) “Certified pharmacy technician” means a person who is certified by the Pharmacy Technician Certification Board (PTCB) or other entity approved by the Board of Pharmacy. The pharmacist-in-charge or applicant must submit the floor plans before any construction and at least 15 days before the next scheduled Board of Pharmacy meeting. (7) “Division” means the Division of Professional Regulation. Laws, c. 167, § 1.; § 2502 Definitions [Effective until July 1, 2021]. Laws, c. 55; 36 Del. You may also visit the Continuing Education and Audit Information webpage. DPH will also receive an additional 3,900 doses of the Pfizer vaccine next week; an additional 6,825 doses of Pfizer will be reserved as part of the federal pharmacy program for vaccinating long-term care residents and staff in the coming weeks, bringing the total of Delaware’s Pfizer allotment for the week of Dec. 21, 2020, to 10,725 doses. The requirements for renewals and continuing education (CE) are found in 24 Del. Laws, c. 95, § 3; 24 Del. Do not create or register an account for yourself in … (14) “Internship” or “externship” means a period of practical experience established by Board of Pharmacy regulation that must be completed by an applicant for a license to practice pharmacy in this State. for Pharmacy – 24 . Three members are public members, 1 from each county. for Controlled Substances o §4701. Delaware Courts Participation in drug utilization and/or drug regimen reviews; b. (c) The Board shall submit a written report to the Governor within 3 months after the conclusion of each fiscal year and shall make the report available to anyone requesting a copy. (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. C. §1731A For information on filing a report, go to the Division’s website at . Laws, c. 238, § 1; 80 Del. Records kept in accord with this section are prima facie evidence of the proceedings of the Board. The consultant pharmacist must notify the Board in writing within ten days of starting as a consultant in Delaware. Wholesale distribution does not include: a. The plans must show that the pharmacy will meet the requirements in the Pharmacy law at 24 Del C. §2533: In addition to the requirements in the law listed above, the plans must show: Note: The Office of Controlled Substances must review and approve the alarm system. An officer may not serve for more than 3 consecutive terms in the same office. Laws, c. 103, § 1; Code 1935, §§ 938, 941, 948, 956; 43 Del. As another reminder, your license expires on September 30. (i) A member who is absent without adequate reason for 3 consecutive regular business meetings or who fails to attend at least 1/2 of all regular business meetings during any calendar year is guilty of neglect of duty. (10) “Executive Secretary” means the executive secretary of the Delaware State Board of Pharmacy who shall be a pharmacist. 2502; Felony: A crime carrying a penalty of more than a year in prison. Members must be appointed so that the terms of no more than 3 members expire in any 1 year. Answer: The Delaware-licensed pharmacist-in-charge (PIC) (or, if the PIC is deceased, another designated Delaware-licensed pharmacist) is responsible for carrying out the closing procedure. (b) A license to practice pharmacy must be renewed biennially, in a manner determined by the Division. Board of Pharmacy. Delaware law recognizes the FDA rating of medication via the Orange Book. Mobile Apps Applications . Submit the following information to the Pharmacy Board office at least 14 days before the planned closing: The PIC (or designated pharmacist) is also responsible for arranging the following: The PIC must also submit the following to the Board of Pharmacy/Office of Controlled Substances: Upon closing, these permits and registrations must be surrendered to the DEA: What are the procedures for drug substitution in Delaware? Personal Income Tax Whether a product can be used as a generic equivalent of a brand name product depends on the rating of the branded product. Laws, c. 167, § 1; 77 Del. ©MMXX Delaware.gov, Professional License Services for Military Personnel, Continuing Education and Audit Information, Controlled Substances Rules & Regulations, Service Request for CE Provider ApprovalÂ, Pharmacist-in-Charge Self-Inspection Report. How do I log into RELIAS to complete my CNA CEUs? 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. For more questions, see Controlled Substances FAQ’s. Transparency This article will explain the requirements and how to … A substance recognized as a drug in the Official United States Pharmacopoeia/National Formulary; b. Mandatory Duty to Report Child Abuse . A Board member may appeal to the Superior Court a suspension or removal initiated pursuant to this subsection. When the FDA has rated a branded drug with an AB rating, you may substitute the generic for the branded drug. State Employees The eLicense Delaware verification is the primary license verification provided by the Delaware Counselor, Social Worker and Marriage & Family Therapist Board. Registration requirements, exemptions, inspections o §4739. A person who is a member of the Board on July 24, 2007, may complete that person’s own term. (9) “Drug outlet” means a pharmacy, an in-state or out-of-state drug wholesaler, a drug manufacturer, a drug distributor, or a nonpharmacy veterinary drug seller. (e) An act or vote on Board business by a person appointed to the Board in violation of this section is invalid. (33) “Telehealth” means the use of information and communications technologies consisting of telephones, remote patient monitoring devices or other electronic means which support clinical health care, provider consultation, patient and professional health-related education, public health, health administration, and other services as described in regulation. mandates Fiscal year: The fiscal year is the accounting period for the government. Upon request a copy of the protocol will be made available to the designated physician or physicians without costs. Search the ... Delaware Administrative Code ••• Title 24 - Regulated Professions and Occupations. Laws, c. 238, § 1; 80 Del. Laws, c. 90, §§ 1, 3; 59 Del. The secondary objective of the Board is to maintain minimum standards of professional competency in the practice of pharmacy. Laws, c. 319, § 1.. DOVER (Dec. 17, 2020) – The Delaware Division of Public Health (DPH) announced it has set up a Vaccine Call Center for members of the public who have specific questions about the COVID-19 vaccine. Gross Receipts Tax The consultant pharmacist must notify the Board in writing within ten days of starting as a consultant in Delaware. This includes, but is not limited to, labeling requirements in 24 Del. Each term of office expires on the date specified in the appointment; however, a Board member whose appointment has expired remains eligible to participate in Board proceedings unless or until replaced by the Governor. Division of Professional Regulation. name, address and phone number of the closing pharmacy. Delaware State Code (19) “Person” means a natural person or an entity. 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. 412, § 1; 74 Del. (5) “Dispense” means to furnish or deliver a drug to an ultimate user by or pursuant to the lawful prescription of a practitioner. Laws, c. 90, § 1; 24 Del. Generic substitution means a drug that is the same active ingredient, equivalent in strength to the strength written on the prescription and which is classified as being therapeutically equivalent to another drug in the latest edition or supplement of the Federal Food and Drug Administration (FDA) Approved Drug Products with Therapeutic Equivalence Evaluations, sometimes referred to as the “Orange Book.”. C. §1731 and 24 . 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. (24) “Practitioner” or “prescriber” means an individual who is authorized by law to prescribe drugs in the course of professional practice or research in any state. (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. Please read the important COVID-19 information from the Division of Professional Regulation More Info. Do I need to reapply for a new license if there is a controlling interest change in ownership of a pharmacy? We are experiencing an unusually high call volume. Forward a copy of this inventory to the attention of OCS in the Division of Professional Regulation. 24 Del. Laws, c. 206, § 1; 76 Del. 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. (29) “State” means the State of Delaware. (21) “Pharmacy” means a place where drugs are compounded or dispensed. Participation in therapeutic drug selection, substitution of therapeutically equivalent drug products; c. Advising practitioners and other health-care professionals, as well as patients, regarding the total scope of drug therapy, so as to deliver the best care possible; e. Performing and interpreting capillary blood tests to screen and monitor disease risk factors or facilitate patient education, the results of which must be reported to the patient’s health-care practitioner; screening results to be reported only if outside normal limits; f. Conducting or managing a pharmacy or other business establishment where drugs are compounded or dispensed; g. The use of telemedicine and participation in telehealth in a manner deemed appropriate by regulation which may not require the use of technology permitting visual communication; and. The Delaware Board of Pharmacy shall prescribe the minimum of such professional and technical equipment which a pharmacy shall at all times possess. Del. All. Pharmacy license number, Controlled Substance registration number and Drug Enforcement Administration registration number, name of the PIC responsible for the closing. General Assembly A person appointed to fill a vacancy on the Board holds office for the remainder of the unexpired term of the vacating member. Answer: Section 3.1 of the Board’s Rules and Regulations explains the requirements and responsibilities of the Pharmacist-in-Charge (PIC). 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. (b) The Board consists of 9 members who are appointed by the Governor and who are residents of the State. Delaware Marketplace 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. C. §2512, Issuance and Renewal of License, and Pharmacy Regulations 1.3 and 1.4. Laws, c. 167, § 1; 79 Del. Privacy Policy The use of prescription drugs without a prescription; or. Agencies; News; Topics; Contact; Effective 10/22/2020 a Security Code is no longer required for registration. Rules and Regulations describes this requirement. Laws, c. 261, § 11; 82 Del. (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. 24 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. (g) A member of the Board, while serving on the Board, may not hold elective office in any professional association of pharmacists or serve as an officer of a professional association’s political action committee (PAC). Laws, c. 366, § 7; 67 Del. 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. § 262). Effective 10/22/2020 a Security Code is no longer required for registration. The Office of the Registrar of Regulations is a section of the Division of Research. (a) The Board of Pharmacy has the authority to: (1) Promulgate rules and regulations in accordance with the procedures specified in the Administrative Procedures Act [Chapter 101 of Title 29]; (2) Designate the application form to be used by all applicants and to process all applications pursuant to this chapter; (3) Designate the national standardized examinations in pharmacy and jurisprudence as approved by the National Association of Boards of Pharmacy, or its successor, to be taken by a person applying for a license to practice pharmacy; (4) Evaluate the credentials of each person applying for a license to practice pharmacy in order to determine whether the person meets the qualifications set forth in this chapter; (5) Grant a license to and renew the license of each person who qualifies for a license to practice pharmacy; and grant or renew a license with restrictions, if appropriate, as a reasonable accommodation to an applicant with a disability; (6) Establish by regulation continuing education standards required for license renewal; (7) Evaluate certified records, including criminal history records, to determine whether an applicant for licensure who previously has been licensed, certified, or registered in another jurisdiction to practice pharmacy has engaged in any act or offense that would be grounds for disciplinary action under this chapter and whether there are disciplinary proceedings or unresolved complaints pending against the applicant for such acts or offenses; (9) Refer all complaints from licensees and the public concerning persons licensed under this chapter, or concerning the practices of the Board or the profession, to the Division for investigation pursuant to § 8735 of Title 29 and assign a member of the Board to assist the Division in an advisory capacity with the investigation for the technical aspects of the complaint; (10) Issue subpoenas to require the attendance of persons and the production of books and papers for the purpose of conducting investigations preliminary to hearings and for the purpose of eliciting testimony at hearings. 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