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).
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Active surveillance means the process of tracking an intruder by using the information gained from the replies to own ACAS interrogations;
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Active surveillance means active measures taken to monitor adverse events
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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 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;
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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;
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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
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Active surveillance means laboratory testing which is conducted during
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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;

  • 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.

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

  • 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