
Get the free CLINICAL LABORATORY ACT - GLOMERULAR FILTRATION ... - legis state pa
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CLINICAL LABORATORY ACT, THE
Act of Sep. 26, 1951, P.L. 1539, No. 389
AN ACT Cl. 35Defining clinical laboratory; regulating the operation of the
same; requiring such laboratories to obtain permits,
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Who needs clinical laboratory act:
01
Clinical laboratory professionals: Clinical laboratory act is particularly relevant for individuals working in clinical laboratory settings such as medical technologists, laboratory technicians, pathologists, and other healthcare professionals involved in laboratory testing and analysis.
02
Healthcare facilities and institutions: Hospitals, clinics, research laboratories, and other healthcare institutions that perform laboratory testing are subject to the clinical laboratory act. Compliance with the act ensures quality and safety in laboratory operations.
03
Regulatory agencies: Government bodies responsible for overseeing and enforcing healthcare regulations are responsible for implementing and enforcing the clinical laboratory act. They ensure that healthcare providers adhere to the laws and guidelines to safeguard public health and welfare.
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What is clinical laboratory act?
The clinical laboratory act is a legislation that outlines regulations and requirements for the operation of clinical laboratories, ensuring accuracy, reliability, and quality in diagnostic testing.
Who is required to file clinical laboratory act?
Clinical laboratories, including medical, dental, and veterinary laboratories, are required to file the clinical laboratory act according to jurisdictional regulations.
How to fill out clinical laboratory act?
Filling out the clinical laboratory act depends on the specific jurisdiction and requirements. Generally, it involves providing information about the laboratory's location, staff qualifications, testing procedures, quality control measures, and compliance with safety standards.
What is the purpose of clinical laboratory act?
The purpose of the clinical laboratory act is to regulate and monitor clinical laboratories to ensure patients receive accurate and reliable diagnostic testing, maintain public health, and protect against fraudulent practices.
What information must be reported on clinical laboratory act?
The required information for the clinical laboratory act varies depending on the jurisdiction but commonly includes laboratory name, address, contact information, testing procedures, staff qualifications, equipment and instruments used, quality control measures, and laboratory director information.
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