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Sections (4.01 - 4.07.2) last updated January 2024.
How to use a before-and-after study to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a quasi-experimental study to evaluate your digital health product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Sections (14.01 - 14.209) last updated: April 2024.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply to appoint your own staff as delegated driving examiners to provide driving tests for your employees of your company, police service or fire and rescue service
Guide to submitting practitioner licence applications to the Administration of Radioactive Substances Advisory Committee (ARSAC).
Training and continuing professional development for people working in the sickle cell and thalassaemia screening programme in England.
A patent registers your invention and lets you take legal action against anyone who makes, uses, sells or imports your invention without your permission.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
Supports effective delivery of planning application process.
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