Active surveillance definition

Active surveillance means laboratory testing which is conducted during the annual hatchery inspection and during spawning as outlined in Chapter 24.21(1)(E), 24.32(4), and 24.34(4).
Active surveillance means prospective measures taken to detect adverse drug reactions and adverse events and involves active follow-up during and after treatment of patients where the events may be detected by asking the patient directly or screening patient records;
Active surveillance means the process of tracking an intruder by using the information gained from the replies to own ACAS interrogations;

Examples of Active surveillance in a sentence

  • Active surveillance for early-stage prostate cancer: review of the current literature.

  • Active surveillance for early-stage prostate cancer: defining the triggers for intervention.

  • Active surveillance using electronic triggers to detect adverse events in hospitalized patients.

  • Active surveillance program for prostate cancer: an update of the Johns Hopkins experience.

  • Active surveillance for the management of prostate cancer in a contemporary cohort.

  • Active surveillance for prostate cancer: a systematic review of the literature.

  • Active surveillance for low-risk prostate cancer worldwide: the PRIAS study.

  • Active surveillance for adverse events: the experience of the Vaccine Safety Datalink project.

  • Roles and responsibilities in Pharmacovigilance.UNIT - VMethods, ADR reporting and tools used in pharmacovigilance:International classification of diseases, International Nonproprietary names for drugs, Passive and Active surveillance, Comparative observational studies, Targeted clinical investigations and Vaccine safety surveillance.

  • Active surveillance for the control of cumulative trauma disorders: A work- ing model in the newspaper industry.


More Definitions of Active surveillance

Active surveillance means active measures taken to monitor adverse events
Active surveillance means active measures taken to monitor adverse events “Law” means Law No. 003/2018 of 09/02/2018 establishing the Rwanda FDA and determining its mission, organization and functioning; “Marketing Authorisation Holder (MAH)” means an individual or corporate entity responsible for placing a pharmaceutical product on the market; “pharmacovigilance (PV)” means the science and activities related to the detection, assessment, understanding and prevention of adverse effects or any other possible medicine-related problems; “post-marketing surveillance” means surveillance activities that occur following market approval of a regulated product including maintenance of product authorisation and/or registration of variations or renewals; regular inspection of manufacturers, wholesalers, distributors and retailers; quality control testing; public reporting of poor quality products; handling of market complaints; and removal and disposal of non-compliant products “Noncompliant products” nonregistered products or noncompliant with specifications including substandard and falsified products. “Substandard products” Also called “out of specification”, these are authorized products that fail to meet either their quality standards or their specifications, or both. “Unregistered/unauthorised products” Pharmaceutical products that have not undergone evaluation and/or approval by the Authority for the market in which they are marketed/distributed or used, subject to permitted conditions under national regulation and legislation. “Falsified products”: that deliberately/fraudulently misrepresent their identity, composition or source. CHAPTER II: POST-MARKETING SURVEILLANCE SYSTEM
Active surveillance means active measures taken to monitor adverse events; “Adverse Drug Reactions (ADRs)” means a response to a medicine which is noxious and unintended, and which occurs at a dose normally used in human for prophylaxis, diagnosis or therapy of disease or for the modification of physiological function;
Active surveillance means laboratory testing which is conducted during

Related to Active surveillance

  • medical surveillance means a planned programme or periodic examination (which may include clinical examinations, biological monitoring or medical tests) of employees by an occupational health practitioner or, in prescribed cases, by an occupational medicine practitioner;

  • market surveillance means the activities carried out and measures taken by public authorities to check and ensure that devices comply with the requirements set out in the relevant Union harmonisation legislation and do not endanger health, safety or any other aspect of public interest protection;

  • Surveillance means monitoring and observation of the disposal site for purposes of visual detection of need for maintenance, custodial care, evidence of intrusion, and compliance with other license and regulatory requirements.

  • market surveillance authority means an authority of a Member State responsible for carrying out market surveillance on its territory;

  • Public safety answering point or “PSAP” means an answering location for 9-1-1 calls originating in a given area. A PSAP may be designated as Primary or Secondary, which refers to the order in which calls are directed for answering. Primary PSAPs respond first; Secondary PSAPs receive calls on a transfer basis only, and generally serve as a centralized answering location for a particular type of emergency call. PSAPs are staffed by employees of Service Agencies such as police, fire or emergency medical agencies or by employees of a common bureau serving a group of such entities.

  • Organ procurement organization means a person designated by the Secretary of the United States Department of Health and Human Services as an organ procurement organization.

  • Environmental Management System means an environmental management system or plan of management to address all environmental risks and to ensure compliance with all Environmental Laws and licences;

  • Environmental and Social Management Plan or “ESMP” means a site-specific environmental and social management plan to be prepared in accordance with the parameters laid down in the ESMF and acceptable to the Association, setting forth a set of mitigation, monitoring, and institutional measures to be taken during the implementation and operation of the Project activities to eliminate adverse environmental and social impacts, offset them, or reduce them to acceptable levels, and including the actions needed to implement these measures.

  • Environmental Management Framework or “EMF” means the environmental management framework dated October 2001, satisfactory to the Association, setting out the principles, policies and procedures for assessing and mitigating the environmental and social impacts of CI schemes, as the same may be amended from time to time with the agreement of the Association;

  • Environmental and Social Management Framework or “ESMF” means the Recipient’s framework to be developed, disclosed and adopted in accordance with the provisions of Section I.D of Schedule 2 to this Agreement.

  • Public safety answering point (PSAP) means a 24-hour, state, local, or contracted communications facility, which has been designated by the local service board to receive 911 service calls and dispatch emergency response services in accordance with the E911 service plan.

  • Public Finance Management Act ’ means the Public Finance Management Act, 1999 (Act No. 1 of 1999);

  • Procurement organization means an eye bank, organ procurement organization, or tissue bank.

  • Review organization means a disability insurer regulated

  • Environmental Management Plan or “EMP” means the environmental management plan for the Project, including any update thereto, incorporated in the IEE;

  • Procurement means the purchasing, buying, renting, leasing, or otherwise obtaining of any supplies, services, or construction. It includes all functions that pertain to the procurement of any supply, service, or construction item, including description of requirements, selection and solicitation of sources, preparation and award of contract, and all phases of contract administration;

  • Monitoring Indicator means a measure of HSP performance that may be monitored against provincial results or provincial targets, but for which no Performance Target is set;

  • Regulatory Floodway means the channel of a river or other watercourse and the adjacent land areas that must be reserved in order to discharge the base flood without cumulatively increasing the water surface elevation more than a designated height.

  • Procurement Manager means any person or designee authorized by a state agency or local public body to enter into or administer contracts and make written determinations with respect thereto.

  • Procurement Process means the process commenced by the issuing of this Invitation and concluding upon the award of a contract (or other outcome as determined by Tetra Tech International Development) or upon the earlier termination of the process

  • 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.

  • Independent review organization means an entity that is accredited to conduct independent external reviews of adverse benefit determinations.

  • Coordinated licensure information system means an integrated process for collecting, storing, and sharing information on nurse licensure and enforcement activities related to nurse licensure laws that is administered by a nonprofit organization composed of and controlled by licensing boards.