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 …

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 …

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 …

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 …

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 …

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 …

2019年4月9日 · In preparation for the possibility of a no-deal Brexit, the UK Medicines and Healthcare products Regulatory Agency has issued guidance on the process for applying for a …

We collected pregnancy pharmacokinetics data from literature and worked on a pregnancy mathematical modelling technique, known as physiologically based pharmacokinetics (PBPK) …

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. ...

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 …