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You can use the PRE service to view recordings of pre-recorded evidence before trial.
Pre-trial proceedings in Bulgaria
Form PRD1 to request the production of documents.
Guidance on labelling for medicinal products used in clinical trials.
How to declare goods that are short shipped on import at temporary storage locations.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology. This is also recommended for all producers as part of their ways...
Application form OC1 for official copies of register/plan or certificate in Form CI.
Check the tariff classification for preparations put up for retail sale.
Guidance on using non-investigational medicinal products in a clinical trial.
Guidance for local authorities and fire and rescue services on the use remediation orders, a Building Safety Act 2022 enforcement power.
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