(1) Applications for registration for a
manufacturer's permit must be filed with the Office of the Georgia State Board
of Pharmacy ("Board") with the required fee.
(2) Registration of a manufacturer will be
considered on the basis of the application filed, fee paid, and a report from
the Director of the Georgia Drugs and Narcotics Agency (GDNA) certifying the
applicant possesses the necessary qualifications for a permit.
(3) Application fees shall NOT be
(4) Permits shall not
be transferable. Permits become null and void upon the sale, or change of mode
of operation of the business, or location of business.
(5) Licenses are renewed for two years and
expire on June 30th of each odd numbered year and may be renewed upon the
payment of the required fee and the filing of an application for renewal. If
the application for renewal is not made and the fee paid before September 1st
of the odd numbered year, the license shall lapse and shall not be renewed, and
an application for reinstatement shall be required. Reinstatement is at the
sole discretion of the Board.
Upon request by the Board or its designee, any manufacturer holding a permit
issued by the Board that causes a dangerous drug or controlled substance
product to be marketed or distributed in this state shall provide, at no cost
to this state, a quantity of one gram or more of the pure compound of each such
product to the Georgia Drugs and Narcotics Agency. Such quantities of pure
compound will only be used for testing and analysis purposes.
(a) All quantities of a pure compound
provided to the Georgia Drugs and Narcotics Agency will be accounted for using
a perpetual inventory system, and a copy of each product inventory will be
available for review by the manufacturer providing the compound upon written
request to the Board.
(b) As the
manufacturer is required by this subsection to submit the dangerous drug or
controlled substance for analysis, the results of any chemical analysis shall
be considered a trade secret within the meaning of Code Section
Ga. Comp. R. & Regs.
Original Rule entitled
"Rules and Regulations Concerning the Chief Drug Inspectors Office" was filed
and effective on June 30, 1965.
Rule repealed and a new Rule entitled "Manufacturer's Permit" adopted.
Filed October 6, 1970; effective
October 26, 1970.
Filed August 2, 1974; effective
August 22, 1974.
Filed March 3, 1977; effective
March 23, 1977.
Filed March 26, 1982; effective
April 15, 1982.
Filed October 18, 1983; effective
November 7, 1983.
New Rule, same title, adopted. F. Aug. 6,
2001; eff. Aug. 26, 2001.
New Rule of same title adopted. F. Feb. 22,
2007; eff. Mar. 4, 2007.
F. Dec. 18, 2014; eff.
Jan. 7, 2015.
Amended: F. June 29,
2015; eff. July 19, 2015.