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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
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Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
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How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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.
E-Zaraat is a IT-based system
How to use usability testing to evaluate your digital health product.
Findings from UNICEF digital inclusion programme for vulnerable Jordanians, Palestinian and Syrian refugees attending Makani centres
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