Sarath Kanekal

President, Regulatory Strategy & Non-Clinical Consultancy

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Position:

President at Regulatory Strategy & Non-Clinical Consultancy

Location:

Greater San Diego Area

Industry:

Pharmaceuticals

Work:

Regulatory Strategy & Non-Clinical Consultancy since Jan 2007
President
Chemgenex Inc Sep 2006 - Dec 2010
Consultant, Nonclinical
SuperGen Feb 2007 - Jan 2009
Executive Director, Preclinical Development
SuperGen Jul 2006 - Feb 2007
Toxicology PK consultant
Chiron (Novartis) Sep 2005 - Oct 2006
Associate Director, Drug Assesment & Development

Education:

American Board of Toxicology 1995 - 2011
DABT, Board Certification in Toxicology Regulatory Affairs Professional Association 2009 - 2010
RAC, Regulatory Affairs The University of Texas at Austin 1990 - 1993
Postdoc, Toxicology University of California, Davis 1984 - 1990
PhD, Pharmacology & Toxicology Madras Veterinary College (TNAU) 1979 - 1984
BVSC (DVM), Vetrinary Medicine & Surgery

Skills:

Oncology
Vaccines
Dermatology
Toxicology
Pain
Life Sciences
IND
Polymers
Stents
Neurology
Therapeutic areas
Infectious Diseases
Rheumatology
Urology
Immunology
Cardiology
Gastroenterology
Endocrinology
Diabetes
Catheters
Hematology
Ophthalmology
Psychiatry
Pharmacology
Clinical Development
Biotechnology

Interests:

Pharmaceutical Toxicology Drug metabolism & disposition Regulatory Affairs Philosophy Photo/videography

Honor & Awards:

Pharmaceutical Manufacturers' Association Fellow (PhRMA Fellow). UC Regents Fellow, University of California, Davis UC Regents Distinguished Scholar, University of California, Davis

President

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Location:

Atlanta, GA

Industry:

Pharmaceuticals

Work:

Regulatory Strategy & Non-Clinical Consultancy since Jan 2007
President
Chemgenex Inc Sep 2006 - Dec 2010
Consultant, Nonclinical
SuperGen Feb 2007 - Jan 2009
Executive Director, Preclinical Development
SuperGen Jul 2006 - Feb 2007
Toxicology PK consultant
Chiron (Novartis) Sep 2005 - Oct 2006
Associate Director, Drug Assesment & Development

Education:

American Board of Toxicology 1995 - 2011
DABT, Board Certification in Toxicology Regulatory Affairs Professional Association 2009 - 2010
RAC, Regulatory Affairs The University of Texas at Austin 1990 - 1993
Postdoc, Toxicology University of California, Davis 1984 - 1990
PhD, Pharmacology & Toxicology Madras Veterinary College (TNAU) 1979 - 1984
BVSC (DVM), Vetrinary Medicine & Surgery

Skills:

Oncology
Vaccines
Dermatology
Toxicology
Pain
Life Sciences
Ind
Polymers
Stents
Neurology
Therapeutic Areas
Infectious Diseases
Rheumatology
Urology
Immunology
Cardiology
Gastroenterology
Endocrinology
Diabetes
Catheters
Hematology
Ophthalmology
Psychiatry
Pharmacology
Clinical Development
Biotechnology
Regulatory Affairs
Glp
R&D
Cro
Regulatory Requirements
Fda
Lifesciences
Clinical Trials
Pharmacokinetics
Gcp
Cancer
Drug Development
Protocol
Assay Development
Biopharmaceuticals
Clinical Study Design
Clinical Pharmacology
Good Clinical Practice
Good Laboratory Practice
U.s. Food and Drug Administration
Cro Management
Fda Gmp
Regulatory Compliance

Interests:

Regulatory Affairs
Drug Metabolism and Disposition
Pharmaceutical Toxicology
Philosophy
Photo/Videography

Sarath Kanekal

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Location:

San Diego, CA

Industry:

Pharmaceuticals

Work:

Education: