Clinical categories definition

Clinical categories means the groups into which hospital treatments are categorised by type, e.g., brain and nervous system, kidney and bladder, and digestive system. At the time of writing there were 38 categories in the Medicare clinical categories system.
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Clinical categories means a group of hospital treatments where all services within a group must be included.
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Examples of Clinical categories in a sentence

  • Next we’ll consider the connectivity problems in two regimes: dense regime and sparse regime.

  • PDPM Clinical Category • Clinical categories are assigned based on the primary diagnosis for the stay • NEW MDS item I0020B (“I-20-B”) is used to then map to one of the PDPM clinical categories.

  • Clinical categories A, B and C are as defined by the CDC www.cdc.gov/mmwr/preview/mmwrhtml/00018871.htm• Category A: Consists of one or more of the CDC defined Category A conditions in a person with documented HIV infection.

  • Bloody or serous nipple discharge 5 = Nipple or areolar scaliness6 = Skin dimpling or retraction7 = Previous normal CBE in past 12 months - CBE not done today 8 = CBE not done today - other or unknown reason9 = CBE refused10 = Discrete palpable mass – previously diagnosed as benign 11 = Focal pain or tenderness Clinical categories - TRANSLATED TO -MDE categories1, 2, 1013, 4, 5, 6, 1127, 8, 95 The CDC understands that category 5 and 6 are not always an indication of breast cancer.

  • Clinical categories are defined by the Department of Health and further specifics of the scope of cover for each clinical category can be accessed on our website territoryhealth.com.au/clinical-categories.

  • The Clinical categories are listed on the left side of the screen in the “View” field.

  • Clinical categories are defined by the Department of Health and further specifics of the scope of cover for each clinical category can be accessed on our website territoryhealth.com.au/clinical-categories.Choice of doctor/hospital Ear, nose and throatPublic hospital accommodation as a private patient e.g. damaged ear drum, sinus surgery, removal of foreign bodies andWhat you are covered forThis provides a summary of cover and isn’t intended to be an extensive list of all the services covered.

  • According to the ASWB guide to social work laws, “Experience of at least two years, or 3,000 hours of supervised, post-graduate work experience is required for both the Advanced and Clinical categories of regulation.

  • The categories eligible to stand for election to Senate include those within the Academic, Clinical and Veterinary Clinical categories.

  • Clinical categories of searches by users of the PICO portal (n=13).

Related to Clinical categories

  • Product Category means the applicable category which best describes the product as listed in this Section 94508.

  • Special Category Data means any personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, or trade union membership, and the processing of genetic data, biometric data for the purpose of uniquely identifying a natural person, data concerning health or data concerning a natural person's sex life or sexual orientation.

  • eligible Categories means Categories (1), (2) and (3) set forth in the table in paragraph 1 of Schedule 1 to this Agreement;

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • 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.

  • 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.

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • clinical evidence means clinical data and clinical evaluation results pertaining to a device of a sufficient amount and quality to allow a qualified assessment of whether the device is safe and achieves the intended clinical benefit(s), when used as intended by the manufacturer;

  • Category 3 means an issue that is minor in nature, a clarification, a comment concerning a conflict between documents or within a document, etc.

  • 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.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Special Categories of Data means personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, or trade union membership, and the processing of genetic data, biometric data for the purpose of uniquely identifying a natural person, data concerning health or data concerning a natural person's sex life or sexual orientation;

  • Medical cannabis means the same as that term is defined in Section 26-61a-102.

  • Phase I Clinical Trial means a study in humans which provides for the first introduction into humans of a product, conducted in normal volunteers or patients to generate information on product safety, tolerability, pharmacological activity or pharmacokinetics, or otherwise consistent with the requirements of U.S. 21 C.F.R. §312.21(a) or its foreign equivalents.

  • Medical cannabis card means the same as that term is defined in Section 26-61a-102.

  • Rating Category means one of the generic rating categories of any Rating Agency without regard to any refinement or gradation of such rating by a numerical modifier or otherwise.

  • Phase 2 Clinical Trial means a human clinical trial of a product that would satisfy the requirements of U.S. 21 C.F.R. Part 312.21(b), as amended, and is intended to explore a variety of doses, dose response, and duration of effect, and to generate evidence of clinical safety and effectiveness for a particular Indication or Indications in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Category 4 Data is data that is confidential and requires special handling due to statutes or regulations that require especially strict protection of the data and from which especially serious consequences may arise in the event of any compromise of such data. Data classified as Category 4 includes but is not limited to data protected by: the Health Insurance Portability and Accountability Act (HIPAA), Pub. L. 104-191 as amended by the Health Information Technology for Economic and Clinical Health Act of 2009 (HITECH), 45 CFR Parts 160 and 164; the Family Educational Rights and Privacy Act (FERPA), 20 U.S.C. §1232g; 34 CFR Part 99; Internal Revenue Service Publication 1075 (xxxxx://xxx.xxx.xxx/pub/irs-pdf/p1075.pdf); Substance Abuse and Mental Health Services Administration regulations on Confidentiality of Alcohol and Drug Abuse Patient Records, 42 CFR Part 2; and/or Criminal Justice Information Services, 28 CFR Part 20.

  • 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.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.