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Bring photo ID to vote Check what photo ID you'll need to vote in person in the General Election on 4 July.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Adopted EU recommendation GEN-007. UK approved recommendation UK21/G007 on the issuing of certificates to multiple applicants for the same product.
The MHRA register of licensed manufacturing sites: manufacturer specials - human (MS) and manufacturer specials authorisation - veterinary (MANSA) only.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Public list of companies in the UK who have had their licence/registration to manufacture or wholesale medicines/ingredients revoked or suspended.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
List of sites granted a manufacturer or wholesale dealer licence
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Estimates for UK manufacturers' sales by product (ProdCom) for 2021, including 2020 final sales data.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
To apply for a manufacturer licence, complete the appropriate form. Applications for a manufacturer licence will be payable on invoice.
Managing waste, health and safety, regulations
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