Article 6 - General Requirements

California Business and Professions Code — §§ 4100-4107.5

Sections (9)

Amended by Stats. 2017, Ch. 598, Sec. 6. (SB 752) Effective January 1, 2018.

Within 30 days after changing his or her address of record with the board or after changing his or her name according to law, a pharmacist, intern pharmacist, technician, designated representative, designated representative-3PL, or designated representative-reverse distributor shall notify the executive officer of the board of the change of address or change of name.

Amended by Stats. 2014, Ch. 507, Sec. 11. (AB 2605) Effective January 1, 2015.

(a)A pharmacist may take charge of and act as the pharmacist-in-charge of a pharmacy upon application by the pharmacy and approval by the board. A pharmacist-in-charge who ceases to act as the pharmacist-in-charge of the pharmacy shall notify the board in writing within 30 days of the date of that change in status.
(b)A designated representative or a pharmacist may take charge of, and act as, the designated representative-in-charge of a wholesaler or veterinary food-animal drug retailer upon application by the wholesaler or veterinary food-animal drug retailer and approval by the board. A designated representative-in-charge who ceases to act as the designated

representative-in-charge at that

entity shall notify the board in writing within 30 days of the date of that change in status.

(c)A designated representative-3PL may take charge of, and act as, the responsible manager of a third-party logistics provider upon application by the third-party logistics provider and approval by the board. A

responsible manager who ceases to act as the responsible manager at that entity shall notify the board in writing within 30 days of the date of that change in status.

Added by Stats. 2025, Ch. 196, Sec. 28. (AB 1503) Effective January 1, 2026.

(a)(1) As provided in this section, all facilities licensed by the board shall complete the self-assessment process by July 1 of every odd-numbered year, unless otherwise established in this section.
(2)The self-assessment process shall be completed on a form provided by the board pursuant to this section.
(b)The form shall be completed to assess the facility’s compliance with federal and state laws identified on the form. For each “no” response, the facility shall undertake a written corrective action or action plan to come into compliance with the law.
(c)(1) The form shall be signed under penalty of perjury by the designated individual, pursuant to this section, and cosigned by the owner or authorized officer of the facility acknowledging they have read, reviewed, and completed the self-assessment to the best of their professional ability and acknowledge that failure to correct any deficiency identified could result in action by the board.
(2)The completed form shall be kept on file in the facility and made available to the board or its designee upon request.
(d)The facility shall use the appropriate designated form based on the type of license, as described in this subdivision and as posted on the board’s internet website.
(1)The Community Pharmacy Self-Assessment/Hospital Outpatient Self-Assessment form shall be completed by the pharmacist-in-charge. In addition to the requirements in subdivision (a), the form shall be completed within 30 days of any of the following:
(A)A new pharmacy license is issued.
(B)There is a change of pharmacist-in-charge, and they become the new pharmacist-in-charge of a pharmacy.
(C)There is a change in the location of a pharmacy to a new address.
(2)The Hospital Pharmacy Self-Assessment form shall be completed by the pharmacist-in-charge. In addition to the requirements in

subdivision (a), the form shall be completed within 30 days of any of the following:

(A)A new pharmacy license is issued.
(B)There is a change of pharmacist-in-charge, and they become the new pharmacist-in-charge of a pharmacy.
(C)There is a change in the location of a pharmacy to a new address.
(3)The Automated Drug Delivery System Self-Assessment form shall be completed by the pharmacist-in-charge of the pharmacy operating the system. In addition to the requirements in subdivision (a), the form shall be completed within 30 days of any of the following:
(A)A new pharmacy license is

issued.

(B)There is a change of pharmacist-in-charge, and they become the new pharmacist-in-charge of a pharmacy.
(C)There is a change in the location of a pharmacy to a new address.
(4)The Compounding Self-Assessment form shall be completed by the pharmacist-in-charge of each pharmacy that compounds drug products. In addition to the requirements in subdivision (a), the form shall be completed within 30 days of any of the following:
(A)A new pharmacy license is issued.
(B)There is a change of pharmacist-in-charge, and they become the new pharmacist-in-charge of a pharmacy.
(C)There is a change in the location of a pharmacy to a new address.
(5)The Surgical Clinic Self-Assessment form shall be completed by the consulting pharmacist of the surgical clinic and cosigned by the professional director.
(6)The Wholesaler/Third-Party Logistics Provider Self-Assessment form shall be completed by the designated representative-in-charge or the wholesaler or responsible manager of the third-party logistics provider. In addition to the requirements in subdivision (a), the form shall be completed within 30 days of any of the following:
(A)A new license is issued.
(B)There is

a change of designated representative-in-charge or responsible manager, and they become the new designated representative-in-charge or responsible manager.

(C)There is a change in the location to a new address.
(7)The Outsourcing Facility Self-Assessment form shall be completed by the designated quality control personnel. In addition to the requirements in subdivision (a), the form shall be completed within 30 days of any of the following:
(A)A new license is issued.
(B)There is a change in the designated quality control personnel.
(C)There is a change in the location to a new

address.

Amended by Stats. 1997, Ch. 549, Sec. 59. Effective January 1, 1998.

Notwithstanding Section 2038, or any other provision of law, a pharmacist may take a person’s blood pressure and may inform the person of the results, render an opinion as to whether the reading is within a high, low, or normal range, and may advise the person to consult a physician of the person’s choice. Pharmacists rendering this service shall utilize commonly accepted community standards in rendering opinions and referring patients to physicians. Enforcement of this section is vested in the Board of Pharmacy of the State of California. Any pharmacist who performs this service shall not be in violation of Section 2052.

Amended by Stats. 2011, Ch. 646, Sec. 1. (SB 431) Effective January 1, 2012.

(a)Every pharmacy shall have in place procedures for taking action to protect the public when a licensed individual employed by or with the pharmacy is discovered or known to be chemically, mentally, or physically impaired to the extent it affects his or her ability to practice the profession or occupation authorized by his or her license, or is discovered or known to have engaged in the theft, diversion, or self-use of dangerous drugs.
(b)Every pharmacy shall have written policies and procedures for addressing chemical, mental, or physical impairment, as well as theft, diversion, or self-use of dangerous drugs, among licensed individuals employed by or with the pharmacy.
(c)Every pharmacy shall report and provide to the board, within 14 days of the receipt or development thereof, the following information with regard to any licensed individual employed by or with the pharmacy:
(1)Any admission by a licensed individual of chemical, mental, or physical impairment affecting his or her ability to practice.
(2)Any admission by a licensed individual of theft, diversion, or self-use of dangerous drugs.
(3)Any video or documentary evidence demonstrating chemical, mental, or physical impairment of a licensed individual to the extent it affects his or her ability to practice.
(4)Any video or documentary evidence demonstrating theft, diversion, or self-use of

dangerous drugs by a licensed individual.

(5)Any termination based on chemical, mental, or physical impairment of a licensed individual to the extent it affects his or her ability to practice.
(6)Any termination of a licensed individual based on theft, diversion, or self-use of dangerous drugs.
(d)The report required in subdivision (c) shall include sufficient detail to inform the board of the facts upon which the report is based, including an estimate of the type and quantity of all dangerous drugs involved, the timeframe over which the losses are suspected, and the date of the last controlled substances inventory. Upon request of the board, the pharmacy shall prepare and submit an audit involving the dangerous drugs suspected to be missing.
(e)Anyone making a report authorized or required by this section shall have immunity from any liability, civil or criminal, that might otherwise arise from the making of the report. Any participant shall have the same immunity with respect to participation in any administrative or judicial proceeding resulting from the report.

Amended by Stats. 2025, Ch. 196, Sec. 29. (AB 1503) Effective January 1, 2026.

(a)All records or other documentation required to be maintained pursuant to this chapter by any entity licensed by the board shall be retained on the licensed premises in a readily retrievable form.
(b)The licensee may remove the original records or documentation from the licensed premises on a temporary basis for license-related purposes. However, a duplicate set of those records or other documentation shall be retained on the licensed premises.
(c)The records required by this

chapter shall be retained on the licensed premises for a period of three years from the date of making. Paper records may be converted into a digital format and maintained only in a noneditable format. Certification that the digitized documents have not been altered may be required by the board.

(d)(1) Any records that are maintained electronically shall be maintained so that the pharmacist-in-charge, or the pharmacist on duty if the pharmacist-in-charge is not on duty, shall, at all times during which the licensed premises are open for business, be able to produce a hardcopy, digitized copy, or electronic copy of all records required by this chapter to be maintained electronically.
(2)In the case of a veterinary

food-animal drug retailer, wholesaler, or third-party logistics provider, any records that are maintained electronically shall be maintained so that the designated representative-in-charge or the responsible manager, or the designated representative on duty or the designated representative-3PL on duty if the designated representative-in-charge or responsible manager is not on duty, shall, at all times during which the licensed place of business is open for business, be able to produce a hardcopy, digitized copy, or electronic copy of all records of acquisition or disposition or other drug or dispensing-related records maintained electronically.

(e)(1) Notwithstanding subdivisions (a), (b), and (c), the board may, upon written request, grant to a licensee a waiver of the requirements that the records described in

subdivisions (a), (b), and (c) be kept on the licensed premises.

(2)A waiver granted pursuant to this subdivision shall not affect the board’s authority under this section or any other provision of this chapter.
(f)When requested by an authorized officer of the law or by an authorized representative of the board, the owner, corporate officer, or manager of an entity licensed by the board shall provide the board with the requested records within three business days of the time the request was made. The entity may request in writing an extension of this timeframe for a period not to exceed 14 calendar days from the date the records were requested. A request for an extension of time is subject to the approval of the board. An extension shall be deemed approved if the board fails

to deny the extension request within two business days of the time the extension request was made directly to the board.

Amended by Stats. 2005, Ch. 621, Sec. 51. Effective January 1, 2006.

For purposes of license verification, a person may rely upon the licensing information as it is displayed on the board’s Internet Web site that includes the issuance and expiration dates of any license issued by the board.

Amended by Stats. 2017, Ch. 548, Sec. 6. (AB 401) Effective January 1, 2018.

(a)The board shall not issue more than one site license to a single premises except as follows:
(1)To issue a veterinary food-animal drug retailer license to a wholesaler pursuant to Section 4196.
(2)To issue a license to compound sterile drugs to a pharmacy pursuant to Section 4127.1 or 4127.2.
(3)To issue a centralized hospital packaging license pursuant to Section 4128.
(4)To issue licenses to two independently owned clinics that share a clinic office space pursuant to Section 4180.5.
(b)For the purposes of this subdivision, “premises” means a location with its own address and an independent means of ingress and egress.

Added by Stats. 2014, Ch. 507, Sec. 13. (AB 2605) Effective January 1, 2015.

If a manufacturer, wholesaler, third-party logistics provider, or pharmacy has reasonable cause to believe that a dangerous drug or dangerous device in, or having been in, its possession is counterfeit or the subject of a fraudulent transaction, the manufacturer, wholesaler, third-party logistics provider, or pharmacy shall notify the board within 72 hours of obtaining that knowledge. This section shall apply to any dangerous drug or dangerous device that has been sold or distributed in or through this state.