Gal Friedman Email
Regulatory Affairs Lead @ アステラス製薬（株）
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Gal Friedman Location
- Israel
Gal Friedman Work
- Regulatory Affairs Lead @ (November 2019 - Present)
- Head Of Regulatory Affairs @ (April 2017 - November 2019)
- RA and PV manager @ (April 2015 - March 2017)
- Pharmacovigilance and RA Manager, GMP-Qualified Person, QPPV @ (December 2010 - May 2015)
- Pharmacovigilance associate @ (November 2007 - December 2010)
Gal Friedman Education
- The Hebrew University of Jerusalem
- Tel Aviv University
- The Hebrew University of Jerusalem
QP certificate (GMP Qualified Person training course)
2012 -
Eudravigilance user certificate (Eudravigilance training course)
2011 -
XEVMPD user certificate (XEVMPD training course)
2011
Gal Friedman Skills
- Biotechnology
- Pharmacovigilance
- Regulatory Affairs
- MedDRA
- Clinical Development
- Lifesciences
- Clinical Trials
- Regulatory Submissions
- Pharmaceutical Industry
- GCP
- Sop
- Pharmacology
- Drug Development
- Medical Writing
- CTMS
- ICH-GCP
- Regulatory Requirements
- Drug Safety
- Biopharmaceuticals
- CRO
- Therapeutic Areas
- 21 CFR Part 11
- Clinical Monitoring
- Pharmaceutics
- FDA
- Public Speaking
- Sales
- Microsoft Word
- PowerPoint
- Microsoft Excel
- Ich Gcp
Gal Friedman Summary
- Gal Friedman, based in Israel, is currently a Regulatory Affairs Lead at Astellas Pharma. Gal Friedman brings experience from previous roles at Bayer, KAMADA, Neurim Pharmaceuticals Ltd and Teva Pharmaceuticals. Gal Friedman holds a The Hebrew University of Jerusalem. With a robust skill set that includes Biotechnology, Pharmacovigilance, Regulatory Affairs, MedDRA, Clinical Development and more. Gal Friedman has 2 emails on RocketReach.
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