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drug clinical trial

  

clinical trial

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Good Clinical Practice

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medication risk assessment survey

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pharmacodynamics

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prescription drug

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drug formulation

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Drug Clinical Trial Experts

The following experts are available as drug clinical trial consultants and drug clinical trial expert witnesses.  Intota experts are peer-recommended authorities who have been carefully selected and rigorously screened.
    Definition:  Drug Clinical Trial - A clinical trial that is performed on a drug.

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Join our distinguished experts for drug clinical trial jobs, projects and consulting opportunities.


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Drug Clinical Trial Experts
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Expert in endocrinology, human physiology, heart disease, diabetes, obesity, and clinical trials
Expert is clinically trained as an Endocrinologist, and performs research in human physiology and clinical trials. The basis of his work is in moving discoveries from the concept stage into human testing, often undertaking first-in-human studies or ... See full profile

Canada

Expert in Trandermal development including INDs, ANDAs, NDAs, MAAs, CMC, preclinical, clinical, bioequivalence
I have been involved in transdermal product development for 15 years and have spearheaded the development of quality control, quality assurance, regulatory affairs and clinical research departments. Among my activities are: 1. See full profile

Florida (FL), USA

Expert in Clinical Development, Orphan Drugs, Regulatory Development
Following more than 25 years in the pharmaceutical industry (Big Pharma, Contract Research Organizations, Small Pharma), Expert has accumulated experience from several hundred clinical studies, primarily in Phase I/Phase II ("First-in-Human", ... See full profile

Siena, Italy

Expert in Clinical Trials, Drug Development, Medical Monitoring, AIDS, FDA Regulation, Safety Assessment
Expert is a public health professional who has extensive international and domestic experience. She has worked for pharmaceutical/biotech companies, hospitals, public health institutions, non-profit organizations, in the areas of clinical trials ... See full profile

California (CA), USA

Expert in Pharmaceutical Development, strategy planning and execution
Expert graduated in Biology at the University of Utrecht, The Netherlands, in 1984. From 1985-89 he was a PhD student at the University of Basel. The research in the field of gene regulation was carried out at the Friedrich Miescher Institute (FMI; ... See full profile

Switzerland

Expert in Regulatory Sub. NDS, ANDS, SANDS, NC, Cross References, Natural Health Products, Medical Devices
Expert's firm has extensive expertise in regulatory submission. They provide different regulatory strategies to their customer's and prepare all types of submissions on their behalf. Expert also has extensive expertise in Narcotic's regulations. See full profile

Quebec, Canada

Expert in Pharma-BioTech Clinical Trial Development and Drug Safety, Medical Monitor
Expert received her M.D. degree from the University of Utah School of Medicine in 1988. She then completed training to practice in remote rural communities through a program at the McKay Dee Hospital for three years as a board certified Family ... See full profile

California (CA), USA

Expert in Pharma/Biotech Development, Life-Cycle Management, 505(b)(2), Chemical Development, CRO Services
Expert is a Pharmaceutical development leader with ~25 years drug development and manufacturing experience with large Pharma, large Biotech, and a highly successful small start-up. Managed large groups (from three different countries), teams and budgets. See full profile

Illinois (IL), USA

Expert in Clinical Pharmacology of Abused Drugs
Expert received his MD degree from the University of Illinois College of Medicine in 1963. He completed his rotating internship and postdoctoral research training in Neuropharmacology in 1965. After completing his training, Expert served as a ... See full profile

Maryland (MD), USA

Expert in Clinical Development
Expert is a Clinical Development executive with over 13 years of expertise and experience in the pharmaceutical industry. Proven track record of successfully managing large budgets with multiple programs and taking drugs from Phase I to Health ... See full profile

Switzerland

Expert in Psychopharmacology in Historical Perspective, Regulatory Behavior, etc.
Over the past 20 years he has done extensive research on the history of drug discovery, drug development, drug registration, and the use of psychopharmaceuticals in medical practice. Among the documents he has collected are the virtually complete set of ... See full profile

Wisconsin (WI), USA

Expert in Biostatistics, Epidemiology, Methodology, Mental Health, Police Procedures, Drug Safety, Malpractice
As a Professor of Statistics, Epidemiology, Public Health and Psychiatry for the last 30 years he has taught, applied and consulted on all of these methods. First trained as public health physician, he did his graduate work (MS and PhD) in the Division of ... See full profile

Arizona (AZ), USA

Expert in Clinical Development Processes and Clinical Trial Technologies
Expert has worked extensively in bringing technology solutions to solve inherent problems of clinical trial processes. The software products he has worked on ranges from 'electronic data collection' to 'document centric' solutions to reduce overall time it ... See full profile

New Jersey (NJ), USA

Expert in Clinical Trial, Biomarker, Clinical Development, Drug Safety, Medical Affairs, Commercialization
As a prescribing physician and a physician in drug development for many years, Expert has expertise in drug mechanism of action and clinical data, and clinical use. Expert is an expert in drug clinical development from planning to protocol design, ... See full profile

Massachusetts (MA), USA

Expert in Pharmaceutical Drug Development, Strategic Executive Management, Biopharma Mergers and Acquisitions
Expert has over 20 years of experience. He is extensively active and has significant experience and expertise in Europe and the US in the areas of drug development and financing throughout Europe and the US. He was responsible for the overall ... See full profile

Netherlands

Expert in Analytical Chemistry, Analytical Technology Development and Application
Expert is a Ph.D. Pharmaceutical Analytical Chemist with extensive experience in separations (LC, GC, Prep GC), dissolution, automation (robotics, computers) and general analytical technologies. He has familiarity with NDA programs and marketed product ... See full profile

Florida (FL), USA

Expert in Design and Conduct of Clinical Trials for Oral Healthcare Products
Expert is a trained periodontist with a career in both academics and industry. He was the senior director of dental affairs and new technology at Warner-Lambert (later Pfizer) consumer health products R&D for close to 15 years. See full profile

New Jersey (NJ), USA

Expert in Pharmaceutical Regulatory Affairs and Quality Compliance
Expert provides regulatory consulting services to the pharmaceutical, biologics, medical device and food industry to assure compliance with U.S. Food and Drug Administration (FDA) Good Manufacturing Practices (GMPs), Good Clinical Practices (GCPs), ... See full profile

Indiana (IN), USA

Expert in Practical Application of GLP, GCP, and cGMP to Pharmaceutical, Device, and Biotechnology Firms
As Vice President at a pharmaceutical company, Expert formulated eight pharmaceuticals for use in their patented buccal delivery platform technology. Five formulations were acceptable to FDA and were allowed to proceed into ... See full profile

New Jersey (NJ), USA

Expert in Pharmaceutical Product Development, Drug Safety, Regulatory Affairs, Due Diligence
Expert is active in U.K. General Practice with wide therapeutic area knowledge and practical patient prescribing. He has a good understanding of the U.K. health system, formulary adoption, N.I.C.E., and reimbursement. See full profile

Northamptonshire, United Kingdom

Expert in Hematology, Oncology, Geriatrics, Clinical Pharmacology, and Internal Medicine
Expert is board certified in internal medicine, hematology, medical oncology, clinical pharmacology, and geriatrics. He has written over 100 professional articles relative to these specialties but particularly in hematology and oncology. See full profile

Maryland (MD), USA

Expert in Biotechnology & pharmaceuticals: drug development, due diligence, strategy, finance, market analysis
With an MD-PhD, clinical training, ten years of experience analyzing and investing in companies developing drugs, and over three years running a start-up company developing a biologic, Expert has seen the drug and biotechnology industries from many ... See full profile

New Jersey (NJ), USA

Expert in Medical Statistics, with a special interest in Evidence Synthesis and Meta-Analysis
Expert (R) Expert has 30+ years experience as an academic medical statistician. His areas of interest and expertise include clinical trial methodology; he was a member of the UK medicines regulatory body, The Committee on Safety of Medicines. See full profile

United Kingdom

Expert in Pharmaceutical/Biotech Clinical Trials, Regulatory, R&D, Mergers & Acquisitions, Trends, Outsourcing
Expert is Director of Regulatory Affairs and Clinical Trials managing $3.6 billion at at a pharmaceutical company in New York, NY. His expertise is in managing and deploying outsource/insource teams worldwide for multiple clinical trials and ... See full profile

Michigan (MI), USA

Expert in Immunology, Genetics and Immunosuppression, Especially in the Field of Transplantation
Expert has over 35 years experience in immunology research at Universities and Medical Schools in London, Los Angeles, Oxford and Manchester. The major focus of his research has been in organ transplantation (kidney, heart lung and liver), but has ... See full profile

California (CA), USA

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