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These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
A register of agreements relating to exclusion orders made by powers under paragraph 7 of Schedule 3 to The Competition Act 1998.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
How investigators and sponsors should manage clinical trials during COVID-19
Insights into the impacts of the coronavirus (COVID-19) pandemic on industries dependent on in-person contact. Using business turnover estimates from HM Revenue and Customs Value Added Tax (VAT) data, our analysis finds wide-ranging impacts "between" and "within" high-contact service industries....
Guidance for industry on flexible approaches we are taking on good distribution practices.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
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