Примеры использования Reference samples на Английском языке и их переводы на Русский язык
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Data pairs are measured on reference samples.
The costs of test and reference samples has significantly increased in recent years.
Example of a Custom Conversion(Two-Point Method) The data pairs(640 HLD/ 41.5 HRC) and(770 HLD/ 54.5 HRC)were measured on two reference samples made from“special steel”.
Biological reference samples must be provided voluntarily by the family member and on the basis of informed consent.
It is of primary importance that laboratories are able to source test and reference samples of internationally controlled substances from abroad.
The shipping of test and reference samples of controlled substances continues to pose difficulties for the availability of the substances.
If a custom conversion needs to be applied throughout a wide hardness range, several reference samples shall be tested to find a stable basis for interpolation.
Reference samples based on CH 3 NH 3 PbI 3 films delivered just slightly higher performances of 10-12% in the same device configuration.
Appeal inspections: A process where the samples or reference samples from the original inspection should be kept for reevaluation.
Reference samples are to be stored according to OD requirements of manufacturing company during validity period of the certificate according to the contract(agreement).
We produce you will be able to see all the reference samples and find out all the questions that you are interested in product quality and cost;
The majority of countries surveyed do not waive charges related to import/export authorizations and customs duties for drug testing laboratories importing test and reference samples.
In the vast majorityof countries that responded, the import of test and reference samples is not given priority in customs clearance and import authorization processes.
In addition, 2,251 reference samples of drugs under international control were provided to 73 national laboratories and 1,042 field drug-testing kits were provided to the national authorities of 64 countries.
Governments may wish to consider increasing the validity period for import/export authorizations for test and reference samples to a minimum of six months paragraph 19, 2007 Guidelines.
Measuring Reference Samples Sample surfaces must be prepared very carefully and if possible, sample shall met the specific geometries to avoid coupling method.
National authorities, particularly those in countries where access to test and reference samples is limited may wish to consider participating in the ICE programme or similar quality assurance programmes.
Based on input received from national competent authorities and drug testing laboratories,the Board noted that many of the obstacles identified in its 2007 Guidelines continue to impede access to test and reference samples by drug testing laboratories.
The few countries which still prohibit the import of test and reference samples of internationally controlled substances should consider amending their legislation paragraph 19, 2007 Guidelines.
In 2010, legislation to create a centralized genetic databank for genetic profiles obtained from the remains of disappeared persons and biological reference samples obtained from families of disappeared persons came into force.
In response to these continued obstacles to the availability of test and reference samples, the Guidelines also set forth concrete courses of action to be undertaken by Governments to foster and facilitate availability.
Given the high cost of samples, Governments should be further encouraged to reduce oreliminate any fees charged by them related to test and reference samples including those for their export, import and customs clearance.
In the guidelines,the Board identified some of the obstacles to obtaining reference samples in a timely manner that were encountered most frequently by laboratories, and guidance was provided on possible ways to remove those obstacles.
Among the countries allowing the multiple listing of substances within the same form, the vast majority report that this measure does not lead to a reduction of costs when compared to those associated with one request per 2 substance,thus failing to address the financial burden related to the acquisition of test and reference samples.
The majority of laboratories that responded to the survey continue to encounter difficulties in obtaining the test and reference samples that they require, especially when those standards are not available from domestic sources.
The Laboratory distributes reference samples of drugs under international control, and their metabolites and precursors; for most laboratories in developing countries, the Programme is the only source of drug standards.
In some instances, national competent authorities have refused to authorize the import of particular test and reference samples on the basis that this would lead the country to exceed its estimates for the controlled substance in question.
UNDCP continued to acquire reference samples of precursors and illicit drugs to support the analytical functions of drug-testing laboratories and their activities under the International Collaborative Exercises within the International Quality Assurance Programme.
More than 100 individuals and institutions worldwide benefited from assistance, including quality assurance support, guidelines and best practice manuals,training workshops and study tours, reference samples, drug and precursor field identification kits, and scientific expertise in areas related to drug analysis.
Despite the recognition of the importance of ensuring the availability of test and reference samples and the progress having already been made on this issue,many laboratories continue to experience difficulties and/or delays in obtaining all the test and reference samples they require.