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Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Find out about clearance applications and how to apply to HMRC for advance confirmation of an exempt distribution when a company purchases its own shares.
How to apply to appoint your own staff as delegated driving examiners to provide driving tests for your employees of your company, police service or fire and rescue service
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Training and continuing professional development for people working in the sickle cell and thalassaemia screening programme in England.
Sets out process and expectations on planning performance and decision making.
Requesting flexible working, how to make an application, what business reasons an employer can give to reject an application and how to appeal.
This guidance is on a Union making an application to be recognised for collective bargaining
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
The selection criteria used to assess GovTech Catalyst funding applications.
HM Land Registry portal users can use the View Applications service to manage portal applications and correspondence in one place.
All patent applications filed at the IPO are checked to identify any which could be prejudicial to national security or public safety.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
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