Examples of using Control tests in English and their translations into Hungarian
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Financial
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Programming
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Official/political
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Computer
Control tests on the finished product.
The studies described here are distinguished from routine control tests conducted according to specifications.
Control tests on the finished medicinal product.
The production unit is attached to a laboratory, which makes control tests, but also assist in product development.
(g) the control tests referred to in Article 81(1) have not been carried out;
The studies described in thissection are different from the routine quality control tests performed in accordance with the product specifications.
The control tests referred to in Article 127(1) have not been carried out; or.
Anamnesis: acute prostatitis 3 years ago,completely recovered, two control tests showed regular values, no more complaints since then.
With persistent and significant increase in transaminases and changes in other indicators of liver function,the drug should be discontinued and control tests performed.
I take it only 5 weeks, recently there were control tests, which showed that the body's response to the drug is, and therefore, the chance of recovery oh-oh what.
(b) the competent authorities may authorize manufacturers and importers of veterinary medicinal products from third countries, where circumstances so justify,to have certain stages of manufacture and/or certain of the control tests referred to in(a) carried out by third parties;
After months of looking for games, programming and design, we launched the control tests in April 2009 and was officially launched the site the following month.
(e) the control tests referred to in Article 81(1) have not been carried out, or any other requirement or obligation relating to the grant of the manufacturing authorization referred to in Article 44(1) has not been complied with.
The same applies where qualitycontrol of the finished product depends on in-process control tests, particularly if the medicinal product is essentially defined by its method of preparation.
I was persuaded by the results of the completed trial and control tests to show them to my clients, which clearly indicate a very high percentage of the people who were fulfilled from the effects and, what is significant, the lack of any side effects of using the preparation.
Time to show all the skills that are acquired in school for a year,but it will not be boring or hard work control tests, and an interesting research project that everyone should think of himself.
I was persuaded by the results of the completed trial and control tests to show them to my clients, which clearly indicate a very high percentage of the people who were fulfilled from the effects and, what is significant, the lack of any side effects of using the preparation.
The competent authority shall ascertain that the manufacturers of veterinary medicinal products from third countries are able to manufacture the veterinarymedicinal product concerned and/or carry out control tests in accordance with the methods described in the documentation submitted in support of the application in accordance with Article 7(1).
The Operator performs regular pool water quality control tests with an accredited laboratory and brings them to the attention of the Guests by placing them visibly near the reception desk.
The competent authority shall ascertain that the manufacturers of veterinary medicinal products from third countries comply with applicable Union legislation and are able to manufacture the veterinarymedicinal product concerned and/or carry out control tests in accordance with the methods described in the documentation submitted in support of the application in accordance with Article 7(1).
If any irregularities are found with the certified products during control tests, site inspections and market observations by the authorised OEKO-TEX® member institutes this can result in the withdrawal of the existing certificate.
(a) the competent authorities ascertain that the manufacturers and importers of veterinary medicinal products from third countries are able to manufacture them in compliance with the details supplied pursuant to Article 12(3)(d),and/or to carry out control tests in accordance with the methods described in the application documents under Article 12(3)(i);
The same applies where the qualitycontrol of the finished product depends on in-process control tests, particularly if the substance is essentially defined by its manufacturing method.
The same applies where the qualitycontrol of the finished product depends on in-process control tests, particularly if the medicinal product is essentially defined by its method of preparation.
The same applies where the qualitycontrol of the finished product depends on in-process control tests, particularly if the medicinal product is essentially defined by its method or preparation.
The same applies where the qualitycontrol of the finished product depends on in-process control tests, particularly if the substance is essentially defined by its manufacturing method.
In the written declaration of conformity, the applicant also recognises that the OEKO-TEX®Association shall be entitled to carry out control tests on up to two certified products at the cost of the licence holder during the period of validity of the certificate in order to ensure compliance with the guaranteed product quality.
(b) the competent authorities may authorize manufacturers and importers of veterinary medicinal products from third countries, where circumstances so justify,to have certain stages of manufacture and/or certain of the control tests referred to in(a) carried out by third parties; in such cases, checks by the competent authorities shall also be carried out in the establishments concerned.
The competent authority shall ascertain that the manufacturers of veterinary medicinal products from third countries comply with applicable Union law, are able to manufacture the veterinarymedicinal product concerned and/or carry out control tests in accordance with the methods described in the documentation submitted in support of the application in accordance with Article 7(1) and that they minimise environmental pollution.