R.C.S.A. § 21a-408-59
Laboratory requirements
Cite as Conn. Agencies Regs. § 21a-408-59
(a) No laboratory shall handle, test or analyze marijuana unless such laboratory:
(1) Is registered with the department as a controlled substance laboratory;
(2) Is independent from all other persons involved in the marijuana industry in Connecticut,
which shall mean that no person with a direct or indirect interest in the laboratory
shall have a direct or indirect financial interest in a dispensary, dispensary facility,
producer, production facility, certifying physician, certifying APRN, or any other
entity that may benefit from the production, manufacture, dispensing, sale, purchase
or use of marijuana; and
(3) Has employed at least one person to oversee and be responsible for the laboratory
testing who has earned, from a college or university accredited by a national or regional
certifying authority, at least a master’s level degree in chemical or biological sciences
and has a minimum of two years of post-degree laboratory experience, or earned a bachelor’s
degree in biological sciences and has a minimum of four years of post-degree laboratory
experience.
(4) Has provided proof to the department of accreditation in testing and calibration in
accordance with the most current version of the International Standard for Organization
and the International Electrotechnical Commission ("ISO/IEC") 17025 or proof that
the laboratory has applied for accreditation in testing and calibration in the most
current version of ISO/IEC 17025. Any testing and calibration method utilized to perform
a medical marijuana analysis shall be in accordance with the laboratory’s ISO/IEC
17025 accreditation. The accrediting body shall be recognized by International Laboratory
Accreditation Cooperation.
(A) A laboratory applying for authorization to provide medical marijuana analytical tests
shall receive ISO/IEC 17025 accreditation within eighteen months from the date the
laboratory applied for ISO/IEC 17025 accreditation. A laboratory may request, and
the commissioner may grant for good cause shown, additional time for the laboratory
to receive ISO/IEC 17025 accreditation.
(B) A laboratory shall send proof of ISO/IEC 17025 accreditation to the department for
all medical marijuana related analytical test methods for which it has received ISO/IEC
17025 accreditation no later than five business days after the date in which the accreditation
as received.
(C) A laboratory may use non-accredited analytical test methods so long as the laboratory
has commenced an application for ISO/IEC 17025 accreditation for analytical test methods
for medical marijuana analysis. No laboratory shall use non-accredited analytical
test methods for medical marijuana analysis if it has applied for and has not received
ISO/IEC 17025 accreditation within eighteen months. The laboratory may request and
the commissioner may grant for good cause shown additional time for the laboratory
to utilize non-accredited analytical test methods for medical marijuana analysis.
(D) At such time that a laboratory loses its ISO/IEC 17025 accreditation for any medical
marijuana related analytical test methods, it shall inform the department within twenty-four
hours. The laboratory shall immediately stop handling, testing or analyzing marijuana.
(b) A laboratory that transports medical marijuana to or from itself, a producer, dispensary
facility or research program location shall have a transportation protocol approved
by the commissioner.