Okla. Admin. Code § 535:20-3-4
Minimum required information for licensure
Effective Aug 27, 201532 Ok Reg 1233Added at 9 Ok Reg 2145, eff 6-11-92; Amended at 10 Ok Reg 3175, eff 6-25-93; Amended at 18 Ok Reg 2749, eff 7-1-01; Amended at 25 Ok Reg 1772, eff 5-12-08 (emergency); Amended at 26 Ok Reg 2296, eff 7-1-09; Amended at 32 Ok Reg 1233, eff 8-27-15Oklahoma State Board of Pharmacy
(a) A manufacturer applicant must submit a satisfactorily completed Board-approved application together with the required fee.
(1) New applicants shall provide, at least, the following:
- (A) Applicant's full name, all trade or business names used, full business address and telephone number;
- (B) Type of ownership, e.g. individual, partnership, limited liability company or corporation;
(C) Name(s) of the owner(s) of the applicant, including:
- (i) if a person, the name, address, Social Security number and date of birth;
- (ii) if other than a person, the name, address, and Social Security number and date of birth of each partner, limited liability company member, or corporate officer and corporate director and the federal employer identification number;
- (iii) if a corporation, the State of incorporation; and
- (iv) if a publicly traded corporation, the information in (a)(1)(C)(ii) is not required for corporate officers and corporate directors.
- (D) Names of designated representatives and facility managers of the applicant, their Social Security numbers and dates of birth;
- (E) Evidence of criminal background checks and fingerprinting of the applicant, if a person, and of all of applicant's designated representatives and facility managers;
- (F) Proof of licensure by the U.S. Secretary of Health and Human Services, Food and Drug Administration, and, if applicable, by the state where the applicant is located (home state); and,
- (G) Upon the Board's written request, a list of all manufacturers, wholesale distributors, third-party logistics providers and dispensers for whom the manufacturer provides services at such facility.
- (2) Renewal applicants shall provide those items listed above.
- (3) Any other information the Board deems necessary to protect the public health and safety.
- (b) The Board may use an outside agency, such as a National Association of Boards of Pharmacy (NABP), at its discretion, to inspect manufacturers.
Added at 9 Ok Reg 2145, eff 6-11-92
Amended at 10 Ok Reg 3175, eff 6-25-93
Amended at 18 Ok Reg 2749, eff 7-1-01
Amended at 25 Ok Reg 1772, eff 5-12-08 (emergency)
Amended at 26 Ok Reg 2296, eff 7-1-09
Amended at 32 Ok Reg 1233, eff 8-27-15