Oct 2, 2020 01:17
3 yrs ago
5 viewers *
English term

Certificate of Analysis (COA)

GBK English to Albanian Medical Medical (general)
Definition from IPEC Europe:
A document listing the test methods, specification and results of testing a representative sample from the batch to be delivered.
Example sentences:
Growers, extractors, manufacturers and resellers use third-party testing laboratories to analyze several aspects of their products. Most commonly, customers want to confirm THC levels are within the legal limit and the cannabinoid profile is what they want or expect. Following testing, laboratories issue a Certificate of Analysis (COA) that is associated with the product being sold giving confidence to the next user. (News Medical)
Some people are now anonymously calling out the company on Instagram, alleging that they’ve experienced severe health problems after eating F-Factor products — from full-body rashes, to severe gastric distress, and even amenorrhea. Some also claim the products may contain lead and asked F-Factor to release a Certificate of Analysis (COA), which would provide lab results of their products' quality control tests. On Thursday, the company shared a COA of its chocolate fiber/protein powder, showing that the product received a "pass," meaning the number of trace metals in the products was below the legal limit. (Shape)
LGM Pharma has separate procedures for qualified suppliers and new suppliers. The company requires a certificate of analysis (CoA), all shipping documents, and the material safety data sheets from suppliers that have already been audited and qualified, according to Lenox.“With a new supplier or with any concerns, we advise our clients to do the release testing themselves. It can be very dependent on the product and the nature of the relationship with the vendor—their reputation, reliability, qualification status,” he says. (PharmTech)
Proposed translations (Albanian)
5 +2 Certifikata e regjistrimit
Change log

Sep 2, 2020 23:09: changed "Kudoz queue" from "In queue" to "Public"

Oct 2, 2020 01:17: changed "Stage" from "Preparation" to "Submission"

Oct 5, 2020 01:57: changed "Stage" from "Submission" to "Selection"

Oct 6, 2020 06:54: changed "Stage" from "Selection" to "Completion"

Proposed translations

+2
1 day 7 hrs
Selected

Certifikata e regjistrimit

Article 14<br />1. The Minister of Health, based on the proposal of the QKKB and the KNB, orders the registration of the drug.<br />2. After issuing the registration order, the QKKB issues the relevant registration certificate after the payment of the relevant fee has been made, no later than 2 months.<br />3. The registration certificate is valid for a period of 5 years, from the date of issuance of the Minister&#039;s order. This period can be extended through the registration procedure after submitting the application.<br /><br /><br /><br />From:<br />LAW No.9323, dated 25.11.2004<br />&quot;FOR DRUGS AND PHARMACEUTICAL SERVICE&quot;
Example sentences:
"Good manufacturing practice" is that part of the enterprise for quality assurance expressed with the initials GMP (Good Manufacturing Practice), which ensures that pharmaceutical products during the manufacturing process are constantly checked before their release on the market, according to quality standards in accordance with the purpose of their use and the requirements of the certificate of registration. (LAW No.9323, dated 25.11.2004)
Peer comment(s):

agree Sara Brari
2 days 5 hrs
agree Besmira Gjoni
2 days 21 hrs
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4 KudoZ points awarded for this answer.
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