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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to use a quasi-experimental study to evaluate your digital health product.
Information on how the CMA investigated the merger, and how you can find out more.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to use a before-and-after study to evaluate your digital health product.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
How to use a cost utility analysis to evaluate your digital health product.
How to use an ethnographic 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.
To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
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