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17 August 2018 EMA/113700/2008Rev.1 Veterinary Medicines DivisionEudraVigilance Access Policy for Medicines for Veterinary Readopted by the Committee for Medicinal Products for Veterinary Use19 April
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How to fill out eudravigilance access policy for
How to fill out eudravigilance access policy for
01
Access the EudraVigilance website and log in with your credentials.
02
Go to the 'My Account' section and navigate to 'Access Rights'.
03
Click on 'Request New Access' and select the type of access you need.
04
Fill out the required fields such as personal information, organization details, and reason for requesting access.
05
Submit the request and wait for approval from the EudraVigilance administrator.
Who needs eudravigilance access policy for?
01
Pharmacovigilance professionals
02
Medical practitioners
03
Drug regulatory authorities
04
Healthcare institutions
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What is eudravigilance access policy for?
Eudravigilance access policy is for providing access to information regarding the safety and efficacy of medicinal products in the European Union.
Who is required to file eudravigilance access policy for?
Marketing authorization holders and sponsors of clinical trials are required to file eudravigilance access policy.
How to fill out eudravigilance access policy for?
Eudravigilance access policy can be filled out online through the EudraVigilance system using the specific templates provided.
What is the purpose of eudravigilance access policy for?
The purpose of eudravigilance access policy is to ensure transparency and access to information on the safety and efficacy of medicinal products.
What information must be reported on eudravigilance access policy for?
Information such as the procedure for requesting access, contact details, and the conditions for access must be reported on eudravigilance access policy.
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