MedSafe Guidance on Clinical Trials: Application Process
The new article describes in detail the application process to be followed by the interested parties when applying for authorisations in the context of clinical trials.
The new article describes in detail the application process to be followed by the interested parties when applying for authorisations in the context of clinical trials.
The new article explains the requirements pertaining to notifications for clinical trials, as well as the Good Clinical Practice requirements.
The new article clarifies the regulatory requirements related to record-keeping and reporting in the context of clinical trials.
The article highlights the key points related to the regulatory framework for healthcare products in New Zealand
The new article describes in detail the key elements of the regulatory system for healthcare products.
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