EDA
The new article addresses the aspects related to the minimum criteria an adverse reaction report should meet to comply with the respective requirements.
EDA
The new article highlights the aspects related to the vigilance system introduced to ensure the continued safety of medical devices allowed to be marketed and used in the country.
EDA
The document clarifies the aspects related to pharmacovigilance and its importance for ensuring continuous safety of medical devices allowed for marketing and use in the country.
EDA
The article provides a general overview of the existing regulatory framework associated with adverse events.
Africa
This chart lists the pharmaceutical, medical and related regulatory authorities of MENA regulations countries along with links to their relevant websites.
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