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Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
How to use a quasi-experimental study to evaluate your digital health product.
Guidance covering various aspects of pharmacovigilance for authorised and unauthorised medicinal products (Specials and the Early Access to Medicines Scheme (EAMS)).
Actions that trial sponsors should consider to build resilience into clinical trial design
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Guidance primarily aimed at local responders covering some common issues that may arise during the Recovery Phase of an emergency in the UK.
Helping public health practitioners conducting evaluations – using process evaluations to explain how complex interventions work.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
You should get legal advice before applying for intellectual property. Your chances of obtaining intellectual property are much greater if you use an attorney.
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