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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
The Environment Agency has opened a consultation into its ‘minded to’ decision to grant a permit variation to a Yorkshire company.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
An overview of the process by which bills become law.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Helping public health practitioners conducting evaluations – using process evaluations to explain how complex interventions work.
Guidance on the various types of modifications that can be made to a clinical trial approval.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Compulsory and voluntary liquidation, the liquidation process, how liquidation affects company directors and the role of a liquidator
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
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