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The revised form of the Certificate of Compliance is given in the Appendix. The revised form of the Certificate of Compliance shall take effect from 1 Aug 2003 and henceforth supersede the form issued under Circular No RD/E02/2002 dated 30 Dec 2002. If you need clarification please email to EMARDELISE ema.gov.sg. Yours faithfully DY CHIEF EXECUTIVE REGULATION DIVISION Updated 30/06/2004 Particulars of Electrical Installation Name of Consumer Address of Installation Electrical Installation...

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What is certificate of compliance ema?

Certificate of Compliance EMA is a document that confirms that a product meets the regulatory requirements set by the European Medicines Agency (EMA). It is issued to pharmaceutical companies to demonstrate compliance with quality, safety, and efficacy standards.

Who is required to file certificate of compliance ema?

Pharmaceutical companies and manufacturers of medicinal products are required to file a certificate of compliance EMA.

How to fill out certificate of compliance ema?

The certificate of compliance EMA can be filled out by providing the necessary information, such as the product details, manufacturing processes, quality control procedures, and supporting documentation. It should be completed accurately and in accordance with the guidelines provided by the EMA.

What is the purpose of certificate of compliance ema?

The purpose of the certificate of compliance EMA is to ensure that pharmaceutical companies and manufacturers meet the regulatory requirements for the quality, safety, and efficacy of medicinal products. It provides assurance to authorities and healthcare professionals that the products meet the necessary standards.

What information must be reported on certificate of compliance ema?

The certificate of compliance EMA must include information such as the product name, active ingredients, manufacturing site details, batch records, specifications, stability data, and any other relevant information as required by the EMA.

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