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Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Comply with good pharmacovigilance practice and prepare for an inspection.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Licensing requirements for importers and exporters, duty rates, reliefs and import VAT for printed books, newspapers and related products.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Evidence considered by the Scientific Advisory Group for Emergencies (SAGE).
Research, analysis and evaluation working papers produced by or on behalf of HM Revenue and Customs.
An index of publications relating to the Independent Medical Expert Group (IMEG).
Agendas, minutes, reports and updates from Monitor's board and committee meetings.
Summary of the government's ongoing programme of work addressing key issues identified by the DCMS Select Committee’s Inquiry into the Economics of Music Streaming, including an indicative timeline for upcoming milestones.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
This collection brings together all documents relating to BIS research papers.
CoRWM position papers and archive provide our published views on specific topics of interest to our stakeholders.
This collection brings together all documents in the Employment Relations Research Series.
Field inspection reports for the Genetic Modification Inspectorate deliberate release inspection programme in England.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Volume 26 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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