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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.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to select compliance points for the assessment of risks to groundwater from land contamination.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Engage with our reform programme, get involved and stay updated on progress.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This document series contains open letters between the Governor of the Bank of England and the Chancellor of the Exchequer which are exchanged if inflation moves away from the target by more than 1 percentage point in either direction.
Trappers of certain species of mammal must use traps that meet international humaneness standards.
Information for 16 to 19 providers delivering CDF industry placements for the 2022 to 2023 academic year.
How to complete an air emissions risk assessment, including how to calculate the impact of your emissions and the standards you must meet.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
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