2019年4月8日 · You’ll need to submit data about the product you’re applying for at least 2 days before you make your CPP application. You must also email [email protected] to let them know when you’re ...

2016年11月11日 · The manufacturing site must hold a valid certificate of inspection from Medicines and Healthcare products Regulatory Agency (MHRA). The certificate is country and ingredient specific.

2022年10月4日 · Published Register of Electronic Export Certificates Issued by the MHRA (Human) - March 2024 (PDF & XLS). 4 March 2024 Export registers for February 2024 have been uploaded

Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA. Since inspections of manufacturers of active substances are based on risk,...

The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country; [1] it is often mentioned in conjunction with the electronic Common ...

Regulatory Agency (MHRA) The MHRA now issues an electronic monthly register of eCPPs which can assist health authorities if further verification of the authenticity of the eCPP is required. • The eCPP is issued as secure PDF document, and cannot be falsified without the receiving entity not realizing its lack of authenticity.

2024年11月12日 · What is a Certificate of a Pharmaceutical Product (CPP)? The WHO Certification Scheme for a Certificate of Pharmaceutical Product (CPP) is an international voluntary agreement to provide assurance to countries participating in the Scheme, about the quality of pharmaceutical products moving in international commerce.

2023年7月17日 · Get a CPP for a centrally authorised product from 1 January 2021. The way you apply for a Certificate of Pharmaceutical Product (CPP) will not change from 1 January 2021, after the end of the transition period. Youll need to submit data about the product youre applying for at least 2 days before you make your CPP application.

To be completed only by MHRA staff - Application Number: SECTION 1. 1.1. Date of application: 1.2. Applicants own reference number : 1.3. Name and dosage form of the product: 1.4. ... MHRA Licensed CPP Unlicensed app form (November 2010) MHRA Licensed CPP Unlicensed app form (November 2010) Title: 1 Author: ritchie Last modified by: Sandhu, Sach

Due to the restrictions caused by COVID-19, the period of validity GMP and GDP certificates issued by MHRA is automatically extended until the end of 2024, except where clarifying remarks in the...