Medication protocol definition

Medication protocol means a specific group of orders to be used for specific symptoms for specific residents and authorized by a health care provider.
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Medication protocol means the medical treatment plan required by state statute for
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Examples of Medication protocol in a sentence

  • In rare cases, an infection may occur.4. Medication protocol: Any medications prescribed by the RD/Phone coach will require a co-signature by the patient’s primary care provider or medical director.

  • EPI Pens need to be made available by the family and are managed under the Prescription Medication protocol detailed below.

  • ALLERGIES/ASTHMA If your child has allergies, please be sure that this is recorded in your family’s TADS profile, that the office personnel know, your child’s teacher(s) know, and as appropriate, that the kitchen staff knows.EPI Pens need to be made available by the family and are managed under the Prescription Medication protocol detailed below.

  • Medication protocol use should be considered in the context of the clinical situation, safety assurance for the patient/service-user and acceptance of accountability by the health care professional involved.Medication protocols must be developed based on evidence of best practice and supported locally by a multidisciplinary team (i.e., senior doctors, pharmacists, nurses, midwives and health care managers).

  • ALLERGIES/ASTHMA If your child has allergies, please be sure that you:● Record it in your family’s TADS profile● Inform the office personnel● Inform your child’s teacher(s)● Inform the kitchen staff, as appropriateThe family must make EPI Pens available and managed under the Prescription Medication protocol detailed below.

Related to Medication protocol

  • Step therapy protocol means a protocol or program that establishes the specific

  • Protocol means, in respect of any category of object and associated rights to which this Convention applies, the Protocol in respect of that category of object and associated rights;

  • Kyoto Protocol means the protocol to the UNFCCC adopted at the Third Conference of the Parties to the UNFCCC in Kyoto, Japan on 11 December 1997 as may be amended;

  • Medication error means any preventable event that may cause or lead to inappropriate medication use or patient harm, while the medication is in the control of the health care professional, patient, or consumer. Such events may be related to professional practice, health care products, procedures, and systems including, but not limited to: prescribing; order communication; product labeling, packaging and nomenclature; compounding; dispensing; distribution; administration; education; monitoring; and use.

  • Medication means any drug, chemical, compound, suspension, or preparation in suitable form for use as a curative or remedial substance taken either internally or externally by any person.

  • Distribution Protocol means the plan for distributing the Settlement Amount and accrued interest, in whole or in part, as approved by the Courts.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • ERCOT Protocols means the document adopted by ERCOT, including any attachments or exhibits referenced in that document, as amended from time to time, that contains the scheduling, operating, planning, reliability, and Settlement (including Customer registration) policies, rules, guidelines, procedures, standards, and criteria of ERCOT. For the purposes of determining responsibilities and rights at a given time, the ERCOT Protocols, as amended in accordance with the change procedure(s) described in the ERCOT Protocols, in effect at the time of the performance or non-performance of an action, shall govern with respect to that action.

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • technical specification means, with respect to any Software, the document setting forth the technical specifications for such Software and included in the Statement of Work.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Study means the investigation to be conducted in accordance with the Protocol.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Protocols means written directions and orders, consistent with the department’s standard of care, that are to be followed by an emergency medical care provider in emergency and nonemergency situations. Protocols must be approved by the service program’s medical director and address the care of both adult and pediatric patients.

  • Manufacturing Process means any process for—

  • Electronic Product Code™ (EPC) means an identification scheme for universally identifying physical objects via RFID tags and other means. The standardized EPC data consists of an EPC (or EPC identifier) that uniquely identifies an individual object, as well as an optional filter value when judged to be necessary to enable effective and efficient reading of the EPC tags. In addition to this standardized data, certain classes of EPC tags will allow user-defined data. The EPC Tag Data Standards will define the length and position of this data, without defining its content.

  • Functional Specifications means the descriptions of features and functions of the Application as expressly set forth in Quote.

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Brand Name or Equal Specification means a specification which uses one or more manufacturer’s names or catalogue numbers to describe the standard of quality, performance, and other characteristics needed to meet District requirements, and which provides for the submission of equivalent products.

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.

  • Direction-indicator lamp means the lamp used to indicate to other road-users that the driver intends to change direction to the right or to the left;

  • Collaborative pharmacy practice agreement means a written and signed