Work Experience:

Medicines Agency of the Republic of Moldova - Head, Drug Authorization, Clinical Evaluation and Pharmacovigilance Department – 2005- 2011
Responsibilities include: management of the process of drug authorization (including the evaluation of pharmacological part of dossiers), monitoring of clinical trials of pharmaceutical products, management of pharmacovigilance activity in Republic of Moldova.

National Institute of Pharmacy, Chisinau, Moldova, Head, Clinical Evaluation and Pharmacovigilance Centre – 2002-2005 National Institute of Pharmacy, Chisinau, Moldova- Research assistant, Laboratory of Pharmacology – 1996-2002

The State University of Medicine and Pharmacy “Nicolae Testemitanu”, Chisinau, Moldova
Assistant, The Pharmacology and Clinical Pharmacology departament – 1992-1996

Education:

The State University of Medicine and Pharmacy “Nicolae Testemitanu”, Chisinau, Moldova
Faculty General Medicine – 1988-1992

Typer of activity – medicine, scientific research, ethical expertise

Position held - vice president of the National committee for the ethical expertise of the clinical study Republic of Moldova, expert In the Health Evaluation and Accreditation Commission, MHRM, independent expert Approval Commission Transplant Agency RM,

Main specialist within the clinical pharmacology specialist commission, MHRM.

Permanent member of the Committee for Bioethics DH-BIO, Strasbourg, France (designated by order of the Ministry of Foreign Affairs no. 1093-b-168 of 08.10.2012-2014, alternate member-present).

The main activities and responsibilities – Didactic activities - training students, residents and doctors, organizing and conducting the acquisition process, evaluating knowledge, skills and competences, training activities in the field of fundamental and clinical pharmacology (practical hours, courses), developing and drafting instructional-methodical materials;

Expertise activity: the ethical expertise of the clinical trial protocols submitted for approval, the expertise of the drug files submitted for the approval of the marketing authorization, the ethical approval of the sampling of organs for transplantation from living donors.

Clinical activity and consultation- Consulting activity regarding the rational use of medicines in medical institutions.

Expertise and accreditation of public health institutions regarding the activity and quality of medical services.