Avner joined the pharmaceutical industry in Regulatory Affairs as a Qualified Person for Luxembourg Pharmaceuticals in 1997. He served as Regulatory Affairs Manager with Trima Israel, one of the leading generic manufacturers in Israel, followed by 6 years with Pfizer Israel as Regulatory Affairs Manager, Head of Pharmacovigilance and Quality Assurance, and as Director of Clinical Operations before establishing Dor Pharmaceutical Services in 2011.
Avner is well-respected in the Israeli Regulatory Affairs and Clinical Trials communities by regulators and colleagues. He has earned a reputation for integrity and efficient, effective support throughout full project lifecycles and beyond.
Avner is certified as a Registered Pharmacist, Israeli Regulatory Affairs Manager and Israeli Qualified Person. He is also a member of the Pharmaceutical society of Israel and the Israeli PDA (Parenteral Drug Association). He is an Israeli QPPV (Qualified Person for Pharmacovigilance) for global pharmaceutical companies.
Contact with Avner: firstname.lastname@example.org