Code of Maryland Regulations
Title 10 - MARYLAND DEPARTMENT OF HEALTH
Part 3
Subtitle 10 - LABORATORIES
Chapter 10.10.07 - Medical Laboratories-Personnel
Section 10.10.07.02 - Permitted POL and POCL - General Supervisor and Consulting Supervisor
Universal Citation: MD Code Reg 10.10.07.02
Current through Register Vol. 51, No. 19, September 20, 2024
A. Primary Standard. A licensee operating a POL or POCL under a permit shall employ or otherwise engage a qualified general supervisor or consulting supervisor.
B. Standards.
(1) Requirement. A laboratory shall employ or
otherwise engage a qualified general supervisor or consulting supervisor who
shall act in concert with the laboratory director to ensure that the laboratory
complies with the standards and requirements of this chapter.
(2) Qualifications-POL and POCL General
Supervisor. To qualify as a laboratory supervisor in a permitted POL or POCL,
an individual shall be a:
(a) Physician who is
board certified, or eligible to be certified in clinical pathology, and
employed to perform or oversee testing on a full-time or part-time basis in the
laboratory being supervised;
(b)
Technologist as defined in COMAR
10.10.01.03BB and
employed to perform tests at least 1 day a week in the lab being supervised;
or
(c) Technician as defined in
COMAR 10.10.01.03BB and
employed to perform tests on a full-time basis in the lab being
supervised.
(3)
Qualifications-Consulting Supervisor. To qualify as a consulting supervisor of
a POL or POCL, an individual shall be a:
(a)
Technologist as defined in COMAR
10.10.01.03BB who
possesses at least 2 years of work experience in a laboratory that:
(i) Operated under a permit, and
(ii) Performed testing services related to
those offered by the laboratory to be supervised; or
(b) Physician who is board certified, or
eligible to be certified in clinical pathology, and employed to perform or
oversee testing on a full-time or part-time basis in the laboratory being
supervised.
(4)
Supervisory Duties and Responsibilities. A general supervisor or consulting
supervisor shall:
(a) Implement and maintain
the applicable laboratory standards and requirements set forth in this
chapter;
(b) Ensure proper and
reliable test performance, reporting, record keeping, and immediate general and
technical supervision of testing personnel and laboratory services;
(c) Develop, implement, and oversee
maintenance of an internal quality assurance program that includes:
(i) A working quality control program or
system that determines and documents accuracy and precision of all tests
performed,
(ii) Selection and use
of quality control and standard materials for analysis,
(iii) Recording and documenting quality
control data,
(iv) Ongoing analysis
of quality control data, and
(v)
Implementation and maintenance of a specimen documentation and management
system;
(d) Prepare and
maintain a SOPM;
(e) Ensure full
participation in an external proficiency testing program approved by the
Secretary as set forth in COMAR
10.10.05.03B;
(f) Teach proper laboratory techniques,
including the importance of quality control, quality assurance, and proficiency
testing;
(g) Review proficiency
testing results, determine sources of error, and work to correct any
problems;
(h) Review proficiency
testing results, analytical studies and evaluations, and survey reports with
technical personnel to improve test performance and laboratory
services;
(i) Maintain, as part of
laboratory records, a log or other suitable record documenting monthly
consultations with the director and all supervisory activities provided to the
laboratory;
(j) Ensure that
laboratory testing personnel:
(i) Possess the
education, training, and experience required to perform and report laboratory
test results accurately and promptly,
(ii) Are sufficient in number for the scope
and complexity of the services provided,
(iii) Receive regular in-service training and
continuing education appropriate for the scope and complexity of the services
provided, and
(iv) Maintain
competency in performing test procedures and reporting test results;
and
(k) Perform other
duties and responsibilities as delegated and authorized by the director that
may include assisting in:
(i) Developing cost
benefit data,
(ii) Identifying and
recommending adjustments to a laboratory's scope of services, and
(iii) Recommending the purchase or
replacement of test kits, reagents, and equipment.
Disclaimer: These regulations may not be the most recent version. Maryland may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.