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      • Medical (general)
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          • Term
            • Certificate of Analysis (COA)
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          • Definition(s)
            • A document listing the test methods, specification and results of testing a representative sample from the batch to be delivered. IPEC Europe
          • Example sentence(s)
            • 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 by
            • 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 by
            • 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 by
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    • Persian (Farsi)
      • Medical (general)
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          • Term
            • گواهی یا برگه تجزیه و تحلیل.آنالیز
          • Additional fields of expertise
          • Definition(s)
            • برگه آنالیز یا certificate of analysis(COA) همان طوری که از اسمش پیداست، سرتیفیکتی است که توسط مسئول quality assurance (کنترل کیفیت) امضا می‌شود و گواهی می‌دهد که ماده مورد نظر آن ویژگی‌هایی که در برگه آنالیز دکر شده را دارد.در واقع این برگه تا حدودی جواب تست‌هایی که در پیش فرمولاسیون باید انجام دهیم را به ما می‌دهد. surena.ac - by Hamidreza Ghobadi Rad
          • Example sentence(s)
            • برگه آنالیز مواد شیمیایی یک سند معتبر است که در آن یک مقام متخصص، کیفیت و خلوص محصولات دارویی، حیوانی و گیاهی صادر شده را تأیید می کند. برگه آنالیز سندی است که گواهی می دهد کالاهای خاص تحت آزمایش های مشخصی با نتایج مشخص قرار گرفته اند. - kmgostar by Hamidreza Ghobadi Rad
            • ارائه گواهی آنالیز آزمایشگاهی معتبر به درخواست مشتری زعفران امیر بنا به درخواست مشتریان، به آن ها گواهی آنالیز آزمایشگاهی معتبر ارائه می دهد. - amirsaffron by Hamidreza Ghobadi Rad
            • درخواست گواهي كيفيت محصول (Certificate of Analysis) مركز كلكسيون ميكروارگانيسم هاي صنعتي تنها بر اساس درخواست كتبي سازمان ها و مراكز اقدام به صدور گواهي كيفيت محصول مي كند. خواهشمند است در صورت نياز به گواهي كيفيت، حتماً در نامه ارسالي همراه با درخواست سويه، نياز به صدور گواهي كيفيت نيز ذكر شود. در غير اين صورت بر طبق مقرارت درون سازماني پس از خروج محصولات از مركز كلكسيون، بهيچوجه امكان صدور گواهي كيفيت وجود ندا - irost by Hamidreza Ghobadi Rad
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    • Albanian
      • Medical (general)
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          • Term
            • Certifikata e regjistrimit
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          • Definition(s)
            • Article 14 1. The Minister of Health, based on the proposal of the QKKB and the KNB, orders the registration of the drug. 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. 3. The registration certificate is valid for a period of 5 years, from the date of issuance of the Minister's order. This period can be extended through the registration procedure after submitting the application. From: LAW No.9323, dated 25.11.2004 "FOR DRUGS AND PHARMACEUTICAL SERVICE" Law Nr.9323, date 25.11.2004 - by Denis Haska
          • Example sentence(s)
            • "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 by Denis Haska
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