Примери за използване на Study audits на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
Provide information on categories of laboratory inspections/study audits.
General guidance for the conduct of study audits will be found at the end of this Annex.
Specific study audits are also often requested by Regulatory Authorities, and can be conducted independently of test facility inspections.
Inspectors will, while conducting laboratory inspections and study audits, have access to confidential, commercially valuable information.
(national) GLP compliance programme: the particular scheme established by a Member State to monitor GLP compliance by test facilities within its territories,by means of inspections and study audits.
Test facility inspections and study audits inevitably disturb the normal work in a facility.
(National) GLP compliance programme: The particular scheme established by a member country to monitor good laboratory practice compliance by laboratories within its territories,by means of inspections and study audits.
(b) special laboratory inspections/study audits at the request of a regulatory authority- e.g. prompted by a query arising from the submission of data to a regulatory authority.
The purpose of this Annex is to provide guidance for the conduct of laboratory inspections and study audits which would be mutually acceptable to the OECD member countries.
Suspension of laboratory inspections or study audits of a laboratory and, for example and where administratively possible, removal of the laboratory from the(national) GLP compliance programme or from any existing list or register of laboratories subject to GLP laboratory inspections.
The purpose of this part of this Annex is to provide guidance for the conduct of test facility inspections and study audits which would be mutually acceptable to OECD member countries.
(b) provisions for special test facility inspections/study audits at the request of a Regulatory Authority, for example, prompted by a query arising from the submission of data to a Regulatory Authority.
The names of laboratories subject to inspection by a designated authority, their GLP compliance status andthe dates upon which laboratory inspections or study audits have been conducted shall not be considered to be confidential.
Suspension of test facility inspections or study audits of a test facility and, for example and where administratively possible, removal of the test facility from the(national) GLP compliance programme or from any existing list or register of test facilities subject to GLP test facility inspections.
A test facility inspection will usually include a study audit orreview as a part of the inspection, but study audits will also have to be conducted from time to time at the request, for example, of a Regulatory Authority.
In the latter two cases, the(national) GLP monitoring authority should have ultimate responsibility for determining the GLP compliance status of laboratories and the quality/acceptability of a study audit, andfor taking any action based on the results of laboratory inspections or study audits which may be necessary.
Ensure that, unless all commercially sensitive andconfidential information has been excised, reports of laboratory inspections and study audits are made available only to regulatory authorities and, where appropriate, to the laboratories inspected or concerned with study audits and/or to study sponsors.
Completion of inspection or study audit.
Prior to conducting a laboratory inspection or study audit, Inspectors should familiarize themselves with the facility which is to be visited.
The administrative and practical details of a laboratory inspection or study audit should be discussed with the management of the facility at the start of the visit.
Problems, or differences of opinion, between inspectors and test facility management will normally be resolved during the course of a test facility inspection or study audit.
Problems, or differences of opinion,between inspectors and laboratory management will normally be resolved during the course of an laboratory inspection or study audit.
If a test facility inspection or study audit reveals only minor deviations from GLP principles, the facility should be required to correct such minor deviations.
Describe the documents and specimens that will be needed for on-going or completed study(ies)selected for study audit.
Maintain records of test facilities inspected(and their GLP compliance status) and of studies audited for both national and international purposes.
Standards Malaysia should maintain records of test facilities inspected(and their GLP compliance status) and of studies audited for both national and international purposes.
Ensure that inspectorate personnel, including experts under contract, have no financial orother interests in the test facilities inspected, the studies audited or the firms sponsoring such studies, .
Ensure that inspectorate personnel have no financial orother interests in the laboratories inspected, the studies audited or the firms sponsoring such studies, .
A procedure should exist whereby a test facility may make representations relating to the outcome of a test facility inspection or study audit for GLP compliance monitoring and/or relating to the action the GLP Monitoring Authority proposes to take thereon.
When a test facility inspection or study audit has been completed, the inspector should be prepared to discuss his findings with representatives of the test facility at a closing conference and should prepare a written report, i.e., the inspection report.