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EXPERIENCEDRUGSAFETY.COM

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In the field of Drug Safety and PharmacoVigilance. Pharmaceutical Industry and its Contract Research organisations can. Benefit from extensive experience in triage, data entry, data processing. And QC of SAE/AE data (both from clinical trials and spontaneous reports). Assistance can be offered in case submissions (including EudraVigilance. And WebTrader reporting), writing of PSURs, FDA Periodic Reports,. Annual Reports and DSURs.

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In the field of Drug Safety and PharmacoVigilance. Pharmaceutical Industry and its Contract Research organisations can. Benefit from extensive experience in triage, data entry, data processing. And QC of SAE/AE data (both from clinical trials and spontaneous reports). Assistance can be offered in case submissions (including EudraVigilance. And WebTrader reporting), writing of PSURs, FDA Periodic Reports,. Annual Reports and DSURs.
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index | experiencedrugsafety.com Reviews

https://experiencedrugsafety.com

In the field of Drug Safety and PharmacoVigilance. Pharmaceutical Industry and its Contract Research organisations can. Benefit from extensive experience in triage, data entry, data processing. And QC of SAE/AE data (both from clinical trials and spontaneous reports). Assistance can be offered in case submissions (including EudraVigilance. And WebTrader reporting), writing of PSURs, FDA Periodic Reports,. Annual Reports and DSURs.

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experiencedrugsafety.com experiencedrugsafety.com
1

work Experience

http://www.experiencedrugsafety.com/work%20Experience.htm

Work for an International operating CRO, post marketing adverse event handling. Including (electronic) reporting of SARS (EVWeb, WebTrader), PSUR/DSUR writing. And literature searches. Database: ARISg. Work for an International operating CRO, duplicate detection/quality control. Activities in the EudraVigilance database. PharmaNet b.v., Leusden. Senior Safety Associate, post marketing adverse event handling including. Electronic) reporting of SARS (EVWeb, WebTrader), PSUR writing and literature.

2

Experience

http://www.experiencedrugsafety.com/Experience.htm

What can Experience Drug Safety offer:. Various activities in the field of PharmacoEpidemology/Drug Safety. Tasks can include (but are not limited to):. Review of serious adverse experience (SAE) information received from. Investigator sites and adverse experiences (AEs) from post marketing. Sources for completeness and regulatory compliance. Data entry of (S)AEs in various databases. Quality control review of completed individual and periodic safety reports.

3

who monique

http://www.experiencedrugsafety.com/who%20monique.htm

Who is Monique de Vlieger. Monique de Vlieger-Vermeulen was born in The Netherlands. In 1971. She completed the HAVO in Leiden, the Netherlands. And after a start as a secretary she was trained in medical. After almost 10 years with Yamanouchi (currently Astellas), most of the time. As Pharmacoepidemiology officer, working with pre- and post-marketing data,. And 9 years with PharmaNet (currently PharmaNet/i3) as Senior Safety Associate.

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In the field of Drug Safety and PharmacoVigilance. Pharmaceutical Industry and its Contract Research organisations can. Benefit from extensive experience in triage, data entry, data processing. And QC of SAE/AE data (both from clinical trials and spontaneous reports). Assistance can be offered in case submissions (including EudraVigilance. And WebTrader reporting), writing of PSURs, FDA Periodic Reports,. Annual Reports and DSURs.

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