Ana Luisa Vilas Alves
Safety Associate III at CROMSOURCE- Claim this Profile
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Topline Score
Bio
Madelein Schoonhoven
Ana is a very pleasant and cooperative colleague, always willing to support. Ana has a lot of knowledge about Safety regulations (both studies with IMP and medical devices) and European regulatory affairs.
Sandra Bausback-Aballo
I had the pleasure of working with Ana Luisa on a clinical trial project. Ana was extremely responsive to requests, could be trusted to deliver on reports well in advance of the deadline and was extremely collaborative with all levels of team members. Ana is detailed oriented and understood the complexity of regulatory reporting to individual Competent Authorities.
Madelein Schoonhoven
Ana is a very pleasant and cooperative colleague, always willing to support. Ana has a lot of knowledge about Safety regulations (both studies with IMP and medical devices) and European regulatory affairs.
Sandra Bausback-Aballo
I had the pleasure of working with Ana Luisa on a clinical trial project. Ana was extremely responsive to requests, could be trusted to deliver on reports well in advance of the deadline and was extremely collaborative with all levels of team members. Ana is detailed oriented and understood the complexity of regulatory reporting to individual Competent Authorities.
Madelein Schoonhoven
Ana is a very pleasant and cooperative colleague, always willing to support. Ana has a lot of knowledge about Safety regulations (both studies with IMP and medical devices) and European regulatory affairs.
Sandra Bausback-Aballo
I had the pleasure of working with Ana Luisa on a clinical trial project. Ana was extremely responsive to requests, could be trusted to deliver on reports well in advance of the deadline and was extremely collaborative with all levels of team members. Ana is detailed oriented and understood the complexity of regulatory reporting to individual Competent Authorities.
Madelein Schoonhoven
Ana is a very pleasant and cooperative colleague, always willing to support. Ana has a lot of knowledge about Safety regulations (both studies with IMP and medical devices) and European regulatory affairs.
Sandra Bausback-Aballo
I had the pleasure of working with Ana Luisa on a clinical trial project. Ana was extremely responsive to requests, could be trusted to deliver on reports well in advance of the deadline and was extremely collaborative with all levels of team members. Ana is detailed oriented and understood the complexity of regulatory reporting to individual Competent Authorities.
Credentials
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eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD)
European Medicines AgencyJun, 2015- Nov, 2024 -
EudraVigilance & Electronic transmission of ICSRs
European Medicines AgencyApr, 2011- Nov, 2024
Experience
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CROMSOURCE - A ClinChoice Company
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Italy
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Pharmaceutical Manufacturing
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100 - 200 Employee
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Safety Associate III
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Apr 2022 - Present
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Community
