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Information to help you protect, manage and enforce your intellectual property (IP) rights in Indonesia.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
A summary of the techniques and standards you should use to monitor ambient air.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Advice for British people moving to or living in Indonesia, including information on health, driving and residence requirements.
To help you protect, manage and enforce your intellectual property (IP) rights in Indonesia.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives in Great Britain and Northern Ireland.
How you can make sure your ambient air quality monitoring meets appropriate quality assurance requirements.
For manufacturers of long-term samplers and test laboratories who carry out testing of equipment.
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