Independent Clinical Laboratory definition

Independent Clinical Laboratory means a laboratory that performs clinical pathology procedures and that is not affiliated or associated with a Hospital, Physician, or Facility Provider.
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Independent Clinical Laboratory means a facility as defined in the Rules of Alabama State Board of Health, Division of Licensure and Certification, Chapter 420-5-8.
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Independent Clinical Laboratory means any laboratory which operates primarily independent of other health care facilities that are licensed by the Alabama State Board of Health, or hospital laboratories that receive and perform reference work from sources outside of the hospital, and performs diagnostic and medical laboratory procedures upon referral. Independent clinical laboratory shall include laboratories operated by blood banks, plasmapheresis banks, radioisotope facilities, specimen collection stations, and laboratories engaged in manufacturing diagnostic test reagents from human whole blood or whole blood derivatives. Federal and State laboratories shall be excluded from these Rules.
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Examples of Independent Clinical Laboratory in a sentence

  • Ancillary providers include Independent Clinical Laboratory, Durable/Home Medical Equipment and Supplies and Specialty Pharmacy providers.

  • For testing or monitoring requiring blood, either the resident must draw his or her own blood or the blood must be drawn by a physician, an RN or LPN, or a phlebotomist from a licensed Independent Clinical Laboratory.

  • Claims for services provided by independent clinical laboratory, durable medical equipment/medical supply, specialty pharmacy and air ambulance providers are required to be filed as follows: • Independent Clinical Laboratory & Specialty Pharmacy: Claims must be filed with the Blue Cross and/or Blue Shield plan in the state where the referring provider is located.

  • File claims for these providers as follows: • Independent Clinical Laboratory (Lab)- The Plan in whose state the specimen was drawn based on the location of the referring provider.

  • However, there has been a more active line of research on tornado warning polygons, as reviewed in the next section.

  • Independent Clinical Laboratory - a laboratory that performs clinical procedures and that is not affiliated or associated with a Hospital, Physician or Other Provider.

  • Pharmacies that are already enrolled in Medicare as a DMEPOS Supplier or Independent Clinical Laboratory, need to enroll as a Pharmacy or Mass Immunizer to obtain a new Provider Transaction Access Number (PTAN) for vaccine claims.

  • Pharmacies that are already enrolled in Medicare as a DMEPOS Supplier or Independent Clinical Laboratory, need to enroll as a Pharmacy or Mass Immunizer to obtain a PTAN for vaccine claims.

  • The following background is disputed: The Government contends that Dr. Steven Jay Wasserman, a dermatologist, and the Wasserman entities were involved in a kickback scheme with Independent Clinical Laboratory doing business as Tampa Pathology Laboratory (“TPL”) and TPL’s owner, Jose SuarezHoyos, M.D. (“Suarez”).

  • File claims for these providers as follows: • Independent Clinical Laboratory (Lab)- File to the BCBS Plan in whose service area the referring provider is located.


More Definitions of Independent Clinical Laboratory

Independent Clinical Laboratory means any laboratory which operates primarily independent of other health care facilities that are licensed by the Alabama State Board of Health, or hospital laboratories that receive and perform reference work from sources outside of the hospital, and
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Related to Independent Clinical Laboratory

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Independent testing laboratory means an independent organization, accepted by the Contracting Officer, engaged to perform specific inspections or tests of the work, either at the site or elsewhere, and report the results of these inspections or tests.

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Testing laboratory means a laboratory, facility, or entity in the state that offers or performs tests of cannabis or cannabis products and that is both of the following:

  • Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.

  • Dental laboratory means a person, firm or corporation

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Phase I Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of a Product in subjects or that would otherwise satisfy requirements of 21 C.F.R. 312.21(a), or its foreign equivalent.

  • Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Certified laboratory means a laboratory that is on an approved list issued by us.

  • Good Laboratory Practice or “GLP” means the applicable then-current standards for laboratory activities for pharmaceuticals (including biologicals) or vaccines, as applicable, as set forth in the Act and any regulations or guidance documents promulgated thereunder, as amended from time to time, together with any similar standards of good laboratory practice as are required by any Regulatory Authority having jurisdiction over the applicable activity.

  • Phase IV Clinical Trial means a product support clinical trial of a Product commenced after receipt of Regulatory Approval in the country where such trial is conducted. A Phase IV Clinical Trial may include epidemiological studies, modeling and pharmacoeconomic studies, and investigator-sponsored clinical trials studying Product that are approved by the JDC and that otherwise fit the foregoing definition.

  • Phase 2 Clinical Trial means a human clinical trial, for which the primary endpoints include a determination of dose ranges or an indication of efficacy in patients being studied as described in 21 C.F.R. §312.21(b), or an equivalent clinical trial in a country in the Territory other than the United States.

  • Phase 4 Clinical Trial means a Clinical Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.

  • Phase 3 Clinical Trial means a pivotal clinical trial in humans performed to gain evidence with statistical significance of the efficacy of a product in a target population, and to obtain expanded evidence of safety for such product that is needed to evaluate the overall benefit-risk relationship of such product, to form the basis for approval of an NDA and to provide an adequate basis for physician labeling, as described in 21 C.F.R. § 312.21(c) or the corresponding regulation in jurisdictions other than the United States.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • clinical investigation means any systematic investigation in one or more human subjects, undertaken to assess the safety or performance of a device;

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Phase IIb Clinical Trial means a clinical trial of a Product on sufficient numbers of patients that is designed to provide a preliminary determination of safety and efficacy of such Product in the target patient population over a range of doses and dose regimens.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;