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Actions that trial sponsors should consider to build resilience into clinical trial design
Sets out the process for efficient and inclusive consultation of planning applications
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Sets out process and expectations on planning performance and decision making.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Sets out process and expectations on pre-application discussions.
Apply for a grant to train a senior mental health lead to develop your school or college's approach to mental health and wellbeing.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Explains how conditions attached to a planning permission should be used and discharged effectively
Find out the information you must give to customers on food products and how to give it.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to use a before-and-after study to evaluate your digital health product.
This guidance identifies common issues with validation and assessment of clinical trial applications and how to avoid them.
Planning practice guidance on biodiversity net gain. Biodiversity net gain is a way of creating and improving biodiversity by requiring development to have a positive impact (‘net gain’) on biodiversity.
Additional State Pension, also known as the State Second Pension or SERPS, is extra money on top of your basic State Pension.
Emergency planning involves making NHS contingency plans and preparing for specific types of major incidents.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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