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Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Practical steps to manage the risk of online harm if your online platform allows people to interact, and to share text and other content.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Environmental regulations and guidance on offshore oil and gas exploration and production, offshore gas unloading and storage and offshore carbon dioxide storage activities
Provides advice on the key points to take into account on design.
Adapt your technology operations, finance models and cost optimisation techniques to get the most out of the public cloud.
Interested parties can review records of applications and statements submitted to OPRED as required by environmental regulations.
Guidance for buyers and suppliers of cloud technology, digital outcomes, digital specialists, user research participants and labs.
Learn about your responsibilities if you own or manage an online platform or service.
How to use pre-production environments to build and test software: development, integration, staging, shared environments.
The DCMS 5G Programme Industrial 5G Testbeds & Trials grant funding competition has now closed for applications. Officials are currently reviewing proposals.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
This page includes summaries of the winning bids for the Future RAN (FRANC) competition
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Increase sustainability throughout the lifecycle of your technology.
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