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The Marine Management Organisation (MMO) is preparing to help our fishing and seafood industries to be ready to trade successfully in the international marketplace from 1st January 2021.
The process to raise matters in relation to the implementation of environment and labour chapters of a Free Trade Agreement.
Application form PSS1: for use by conveyancers when acting for clients involved in a complex commercial transaction or infrastructure development.
Interested parties can review records of applications and statements submitted to OPRED as required by environmental regulations.
A party seeking an opinion or determination from the SSRO may find it helpful to complete this submission template and return it to referrals@ssro.gov.uk.
You should follow the standard file process outlined below when submitting work for online and paper billing.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
How to apply for marketing authorisation via this new procedure.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
2024 Submissions and Decisions
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guide to the submission process.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
How CWA works online: how to claim, bulkloading, outcomes, new matter starts and guidance.
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