Good Research Practice definition

Good Research Practice means standards, practices, methods and procedures conforming to the applicable laws and regulations and 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 in a similar type of undertaking under the same or similar circumstances.
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Good Research Practice means standards, practices, methods and procedures conforming to the applicable laws and regulations and 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 in a similar type of undertaking under the same or similar circumstances.
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Good Research Practice means all applicable Good Research Practices including, as applicable: (a) the research quality standards defining how Lilly’s research laboratories conduct good science for non-regulated work as set forth in Exhibit 3.6 Part A of this Agreement; (b) the Research Quality Association (RQA), 2014 Quality in Research Guidelines for Working in Non-Regulated Research; (c) the WHO Quality Practices in Basic Biomedical Research Guidelines; or (d) the equivalent applicable guidelines if any, in any relevant country, each as may be amended and applicable from time to time.
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Examples of Good Research Practice in a sentence

  • You should also consult the University’s Code of Good Research Practice to see whether these guidelines raise any issues for your own research, and discuss them with your supervisor.

  • All applicants must read and accept NNF’s Standards for Good Research Practice before submitting the application.

  • The 65 Trial will be sponsored by ICNARC and managed by the ICNARC CTU according to the Medical Research Council’s Good Research Practice: Principles and Guidelines and Scientific Misconduct Policy and Procedure(8), based on the principles of the International Conference on Harmonization guidelines on Good Clinical Practice and the Department of Health’s Research Governance Framework for Health and Social Care.

  • In this case, Dk represents DUSD , DEUR , DGBP : dummy variables for observations of transactions invoiced in theU.S. dollar, the euro and the pound respectively.Figure 6 plots the changes in the log of price and tariff for products invoiced in various currencies.

  • There is an onus on all staff and students to ensure that they are familiar with this Code of Good Research Practice in conjunction with other relevant existing policies and procedures of Dublin City University.

  • Good Research Practice: Principles and Guidelines Secondary Good Research Practice: Principles and Guidelines 2012.

  • In accordance with the University Policy and Guidelines on Good Research Practice (Section 4, above), they indicate that all researchers are required to keep clear and accurate records of the procedures followed and approvals granted during the research process.

  • The methodology was conducted in accordance to standards set by the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA, 2005) and in accordance with the NACD’s Guidelines on Good Research Practice – Research Ethics (2005).

  • Data will be collected, managed and stored in compliance with the requirements of the Joint Code of Practice for Research, MRC’s Good Research Practice, University of Edinburgh’s Research Data Management policy and local protocol documents.

  • This means exhibiting impeccable scientific integrity and following the principles of good research practice detailed in the MRC Good Research Practice Guidelines.All researchers submitting a proposal to MRC must accept the Research Council Terms and Conditions of Research Council fEC Grants and MRC Terms and Conditions.We also expect all stakeholders in fellowships to act in accordance to our Expectations of MRC Fellowships and comply with the guidance in this handbook and the Guidance for Applicants.

Related to Good Research Practice

  • 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.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • 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.

  • Research Program has the meaning set forth in Section 3.1.

  • 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.

  • 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.

  • Research Program Term has the meaning set forth in Section 2.2.

  • Group practice means a group of two or more health care providers legally organized as a partnership, professional corporation, or similar association:

  • Collaborative pharmacy practice agreement means a written and signed

  • Collaboration Know-How means all Know-How conceived, discovered, developed or otherwise made by or on behalf of a particular Party or any of its Affiliates or permitted subcontractors of any of the foregoing (solely or jointly by or on behalf of a particular Party or any of its Affiliates or permitted subcontractors of any of the foregoing) in the course of [***].

  • Research Use shall have the meaning given in Section 2.2.2 of this Agreement.

  • Research Project means a discrete scientific endeavor to answer a research question or a set of research questions related to medical marijuana and is required for a medical marijuana research license.

  • Collaborative practice agreement means a written agreement

  • Good Laboratory Practices or “GLP” means the then-current Good Laboratory Practice (or similar standards) for the performance of laboratory activities for pharmaceutical products as are required by applicable Regulatory Authorities or Applicable Law. In the United States, Good Laboratory Practices are established through FDA regulations (including 21 C.F.R. Part 58), FDA guidance, FDA current review and inspection standards and current industry standards.

  • Research Plan shall have the meaning set forth in Section 2.1.

  • Collaboration has the meaning set forth in Section 2.1.

  • 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.

  • Licensed Practical Nurse (LPN means a Practical Nurse who has completed a certificate program and passed the practical nurse licensure exam as required by the WY State Board of Nursing.

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

  • 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.

  • 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.

  • 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.

  • Good Practice means such practice in the processing of personal data as appears to the Commissioner to be desirable having regard to the interests of data subjects and others, and includes (but is not limited to) compliance with the requirements of this Act;

  • Development Activities means those activities which are normally undertaken for the development, construction, repair, renovation, rehabilitation or conversion of buildings for residential purposes, including the acquisition of property;

  • Licensed Processes means processes which, in the course of being practiced, would be within the scope of one or more claims of the Licensed Patent Rights that have not been held unpatentable, invalid or unenforceable by an unappealed or unappealable judgment of a court of competent jurisdiction.

  • Practice of medicine or osteopathic medicine means the prevention, diagnosis and treatment of