Lev Verkh
CHIEF REGULATORY & CLINICAL DEVELOPMENT OFFICER at Stemedica Cell Technologies, Inc. | San Diego, California, United States
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Dr. Lev Verkh currently serves as the Chief Regulatory & Clinical Development Officer at Stemedica Cell Technologies, Inc., where he leverages nearly three decades of extensive experience in clinical development and regulatory affairs. His role encompasses the strategic oversight of worldwide regulatory processes and clinical development initiatives, ensuring compliance with FDA regulations and international standards. Dr. Verkh has been instrumental in preparing and securing Investigational New Drug (IND) approvals for groundbreaking therapies, particularly in the fields of oncology and regenerative medicine.
Throughout his illustrious career, Dr. Verkh has directed numerous national and multinational Phase I, II, III, and IV clinical trials, showcasing his expertise in navigating complex regulatory landscapes. His previous positions at renowned organizations such as Pfizer, Baxter Bio Sciences, and Alliance Pharmaceutical Corporation have equipped him with a robust understanding of drug development, Good Manufacturing Practices (GMP), and the intricacies of working with Contract Research Organizations (CROs). His experience extends to engaging with foreign regulatory authorities, enhancing his ability to facilitate global clinical trials and product approvals.
At Stemedica, Dr. Verkh is currently focused on innovative projects that aim to advance cell-based therapies for various medical conditions, including cardiology and neurology. His leadership in clinical development not only drives the advancement of novel treatments but also ensures that they meet the highest safety and efficacy standards. With a proven track record in medical imaging applications and a commitment to enhancing patient outcomes, Dr. Verkh continues to be a pivotal figure in the evolution of regenerative medicine.
CHIEF REGULATORY & CLINICAL DEVELOPMENT OFFICER at Stemedica Cell Technologies, Inc. in January 2010 to Present
Consultant, PHARMACOKINETICS & FIRST-in-MAN STUDIES at Pfizer in January 2004 to January 2010
Consultant at Baxter International Inc. in January 2002 to January 2004
DIRECTOR OF CLINICAL RESEARCH at Allience Pharmaceutical Corporation in January 1998 to January 2002
ASSOCIATE DIRECTOR, CLINICAL RESEARCH at Alpha Therapeutic Corporation (Green Cross of Japan) in January 1990 to January 1998
EXECUTIVE OFFICER FOR THE LEUKEMIA INTERGROUP at Roswell Park Memorial Institute, Buffalo, NY in January 1987 to January 1990
DIRECTOR of SURGICAL RESEARCH LABORATORY at Buffalo General Hospital in January 1986 to January 1987
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SUNY at Buffalo, School of Medicine, Doctor of Philosophy (PhD)
University at Buffalo, Master of Science (M.S.)
State University, Odessa, Ukraine, Bachelor of Applied Science (B.A.Sc.)
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Clinical Trials
Clinical Development
Biotechnology
Cardiology
Clinical Research
Lifesciences
Sop
Pharmaceutical Industry
Oncology
Biopharmaceuticals
FDA
GMP
Medicine
Pharmaceutics
Hematology
Life Sciences
Cell
CRO
Drug Development
Regulatory Affairs
GCP
Medical Devices
Neurology
Medical Imaging
Peripheral vascular disease
Foreign contries regulatory authorities experience
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What is Lev Verkh email address?
Email Lev Verkh at [email protected], [email protected] and [email protected]. This email is the most updated Lev Verkh's email found in 2026.
What is Lev Verkh phone number?
Lev Verkh phone number is 4106438641.
How to contact Lev Verkh?
To contact Lev Verkh send an email to [email protected], [email protected] or [email protected]. If you want to call Lev Verkh try calling on 4106438641. (updated on August 26, 2024)
What company does Lev Verkh work for?
Lev Verkh works for Stemedica Cell Technologies, Inc.
What is Lev Verkh's role at Stemedica Cell Technologies, Inc.?
Lev Verkh is CHIEF REGULATORY & CLINICAL DEVELOPMENT OFFICER
What industry does Lev Verkh work in?
Lev Verkh works in the Biotechnology industry.
Lev Verkh Email Addresses
Lev Verkh Phone Numbers
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