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This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for manufacturers, importers and distributors.
Find out about your human rights and how they are protected.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This guide provides information about being arrested in Turkey and what conditions are like in prison there.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
How to write requirements for services on the Digital Outcomes and Specialists framework
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Documents, certificates, letters and notes available from British consulates in Brazil.
Pharmacovigilance system requirements
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
FCDO travel advice for Argentina. Includes safety and security, insurance, entry requirements and legal differences.
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