Approval to Practice definition

Approval to Practice means authorization by the Medical Board and the Board of Nursing for a nurse practitioner to perform medical acts within her or his area of educational preparation and certification under a collaborative practice agreement (CPA) with a licensed physician in accordance with this Subchapter.
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Approval to Practice means authorization by the Joint Subcommittee of the Medical Board and the Board of Nursing for a nurse practitioner to practice within her or his area of educational preparation and certification under a collaborative practice agreement with a physician licensed by the Medical Board in accordance with this Section.
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Approval to Practice means authorization by the Medical Board and the Board of Nursing
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Examples of Approval to Practice in a sentence

  • Either party breaches any of the material provisions of this Agreement and fails to remedy such breach within thirty (30) days after written notification by the other party of such breach.

  • The Mentor also co-signs the Non-Medical Prescriber’s Approval to Practice form to confirm their scope of prescribing practice.

  • This request will come from LCSU.Non-Medical Prescribers - Approval to Practice form/Annual DeclarationThis form must be returned before the non-medical prescriber can be registered with the NHSBSA and prescribe in the practice.

  • The relevant Approval to Practice form should be completed and sent to Chief Pharmacist / Deputy Director of Nursing for final authorisation and updating of the register – as outlined in sections 7 and 10.

  • Registered Practitioners must register their prescribing status with the relevant professional body on successful completion of the prescribing course.Trust support for a non-medical prescriber’s role must then be gained through approval of the Approval to Practice Form (see appendix 5) by NMPG.The area of service provision that the prescriber can work within will be set out in the Approval to Practice Form, and a copy will appear in the staff member’s personal file.

  • MNPs that did not have a satisfactory Approval to Practice form within 12 months of date of issue were not authorised to prescribe.E-learning was utilised and monitored via ESR for safe insulin administration and antimicrobial stewardship.

  • These individuals must complete a period of supervised practice* in their specialist area before submission of the form (see below).Non-medical prescribers approved to practice will receive a letter (Appendix 6) together with a copy of the approved Approval to Practice form.

  • The Approval to Practice form (Appendix 2) should be completed, for each practice the locum non-medical prescriber works in, to enable them to be registered with NHSBSA for their duration of service with the GP practice and allow for monitoring of their prescribing data.

  • Non-medical prescribers new to the Trust who have gained the qualification elsewhere or those who wish to provide a service under a SLA will be required to submit evidence of previous education, training and competence together with the Approval to Practice Form to NMPG.

  • Completing the Approval to Practice form will identify, to the Practice and Mentor, that the Non-Medical Prescriber has the relevant knowledge, competence, skills and experience (including children and controlled drug prescribing).

Related to Approval to Practice

  • Privilege to practice means: an individual's authority to deliver emergency medical services in remote states as authorized under this compact.

  • Community practice protocol means a written, executed agreement entered into voluntarily between an authorized pharmacist and a physician establishing drug therapy management for one or more of the pharmacist’s and physician’s patients residing in a community setting. A community practice protocol shall comply with the requirements of subrule 8.34(2).

  • Development approval means a document from a governmental entity which authorizes the commencement of a development.

  • Collaborative practice means that a physician may delegate aspects of drug therapy management for the physician’s patients to an authorized pharmacist through a community practice protocol. “Collaborative practice” also means that a P&T committee may authorize hospital pharmacists to perform drug therapy management for inpatients and hospital clinic patients through a hospital practice protocol.

  • Active practice means post-licensure practice at the level of licensure for which an applicant is seeking licensure in Virginia and shall include at least 360 hours of practice in a 12-month period.

  • Proper practices means those set out in The Practitioners’ Guide

  • Development Consent means the consent granted to the Development Application for the Development and includes all modifications made under section 4.55 of the Act.

  • Good Manufacturing Practices means current good manufacturing practices, as set forth in 21 C.F.R. Parts 210 and 211.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or more pharmacists have jointly agreed, on a voluntary basis, to work in conjunction with one or more practitioners under protocol whereby the pharmacist may perform certain pharmaceutical care functions authorized by the practitioner or practitioners under certain specified conditions or limitations.

  • Good Industry Practice means standards, practices, methods and procedures conforming to the Law and the exercise of the degree of skill and care, diligence, prudence and foresight which would reasonably and ordinarily be expected from a skilled and experienced person or body engaged within the relevant industry or business sector;

  • Good Manufacturing Practice or “GMP” means the current good manufacturing practices applicable from time to time to the manufacturing of a Product or any intermediate thereof pursuant to Applicable Law.

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Private Practice means those services provided, in or using the hospital's facilities, and for which fees are charged by or on behalf of the practitioner.

  • Best Industry Practice means that degree of skill, care and foresight and operating practice that would reasonably and ordinarily be expected of a skilled and competent supplier of services engaged in the same type of undertaking as that of the Recipient or any contractors (as applicable) under the same or similar circumstances as those contemplated by this Agreement.

  • Best Practice means solutions, techniques, methods and approaches which are appropriate, cost-effective and state of the art (at Member State and sector level), and which are implemented at an operational scale and under conditions that allow the achievement of the impacts set out in the award criterion ’Impact’ first paragraph (see below).

  • Good Clinical Practice or “GCP” means the then current standards for clinical trials for pharmaceuticals, as set forth in the ICH guidelines and applicable regulations promulgated thereunder, as amended from time to time, and such standards of good clinical practice as are required by the European Union and other organizations and governmental agencies in countries in which a Licensed Product is intended to be sold to the extent such standards are not less stringent than the ICH guidelines.

  • Good Clinical Practices means the FDA’s standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials contained in 21 C.F.R. Part 50, 54, 56, 312, 314, 320, 812, and 814 and (ii) “Good Laboratory Practices” means the FDA’s standards for conducting non-clinical laboratory studies contained in 21 C.F.R. Part 58.

  • CPUC Approval means a final and non-appealable order of the CPUC, without conditions or modifications unacceptable to the Parties, or either of them, which contains the following terms:

  • Good Industry Practices means the practices that would be adopted by, and the exercise of that degree of care, skill, diligence, prudence and foresight that reasonably would be expected from, a competent contractor in the international oil and gas industry experienced in performing work similar in nature, size, scope and complexity to the Work and under conditions comparable to those applicable to the Work, where such work is subject to, and such contractor is seeking to comply with, the standards and codes specified in the Contract or (to the extent that they are not so specified) such national or international standards and codes as are most applicable in the circumstances, and the applicable Law.