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drug screening


drug discovery


animal drug testing


employee drug testing


drug blood level determination


medical diagnostic test


driving under the influence testing


active pharmaceutical ingredient


investigational drug procedures






molecular diversity


combinatorial chemistry


pharmaceutical technology


animal disease model


drug formulation


rational drug design


mouse surgery


drug metabolite


blood testing


urine control sample


drug validation


drug clinical trial


drug processing


drug toxicology


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Drug Screening Experts

The following experts are available as drug screening consultants and drug screening expert witnesses.  ORC experts are peer-recommended authorities who have been carefully selected and rigorously screened.
    Definition:  Drug Screening - Preclinical testing of drugs in experimental animals or in vitro for their biological and toxic effects and potential clinical applications

Synonyms:  drug testing, pharmaceutical screening, pharmaceutical testing

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Expert in Medical Pharmacology, Toxicology, Consulting Expert Witness
Expert is a medical-legal consultant who specializes in cases that relate to drugs and drug pharmacology/toxicology. He has over 20 years of experience. Expert has experience in civil, criminal & administrative cases--both plaintiff and defense. Dr. See full profile

Georgia (GA), USA

Expert in Occupational Medicine
Expert is Board Certified by the American Osteopathic Board of Family Physicians in Family Practice and Osteopathic Manipulative Medicine, and has had 25 years of experience in this field. Osteopathic Manipulation is an important part of patient care ... See full profile

Ohio (OH), USA

Expert in Drug Discovery, Neuropharmacology, Serotonin, Dopamine, Antipsychotics, Pharma Project Management
Expert is an industrial neuropharmacologist with seventeen years of proven achievement in preclinical drug discovery of novel antipsychotics, antidepressants and analgesics (examples of drugs characterised: milnacipran, befiradol, F15599, F15063). See full profile


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 Pre-Clinical Pharmacology, Drug Discovery to IND
Expert has been a member of the Faculty of a UK university medical school for 21 years. He is Director of the Cellular and Molecular Neuropharmacology Research Group. The group's principal research interest is 5-HT (5-hydroxytryptamine, serotonin) and ... See full profile

United Kingdom

Expert in Chemistry R&D and cGMP Manufacturing, Pharmaceutical Development
Expert has worked on research, development and manufacturing problems involving stereochemistry throughout his academic training and industrial career. Relevant examples include: development of scalable chiral and asymmetric syntheses; improvement of ... See full profile

Massachusetts (MA), USA

Expert in Antimicrobial Screening, Drug Discovery, Clinical Microbiology, Fermentation Technology
Expert has over ten years of experience in drug discovery with emphasis on screening bioactive natural compounds possessing antimicrobial, antioxidant, anticancer and wound healing activities of plant (Ethnopharmacology / Pharmacognosy) as well ... See full profile

Punjab, India

Expert in Licensing, Biopharma, Pharma, Medical Devices, Chemistry, Agreements, Business Development
Expert has more than 25 years of expertise in transactional and regulatory counseling, acquisition, licensing, due diligence, dispute resolution, opinions, and appeals for the development and commercialization of health care, pharmaceutical, biotechnology, ... See full profile

Colorado (CO), USA

Expert in Occupational and Environmental Medicine
Expert is board certified in Family Practice with a speciality in general practice and a sub-speciality in Occupational Medicine. He has over 20 years of experience in his field, providing high quality occupational medical care to his patients and ... See full profile

Missouri (MO), USA

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 FDA Regulations, GMP/GLP/GCP Compliance; IND, NDA, BLA, PMA and Product Regulation; Toxicology
Experienced in all aspects of validation and compliance including, GMP/GLP/GCP and part 11. Expert worked for over five years as a reviewer of investigational new drug applications, marketing applications, developing guidance and government policy and ... See full profile

California (CA), 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


Expert in Biomaterials: Biocompatibility, Pathology, Devices
Expert is a D.V.M. with a Ph.D. in veterinary pathology. He is also board certified by the American College of Veterinary Pathologists. As part of his Ph.D. research training he was involved in the characterization of several spontaneous large ... See full profile

North Carolina (NC), USA

Expert in FDA Compliance, Pharmaceutical New Products, Management Training, Seminars, Inspections, Audits
During his employment with the Food and Drug Administration, Expert received five grade promotions, with his last position being that of Director of the Science Branch of the Philadelphia District. Expert's area of responsibility included all the ... See full profile

Georgia (GA), USA

Expert in Controlled Substances, Blood/Breath Alcohol, Urine Drug Screen Issues, Chain of Custody, Chemistry
Expert has been involved in forensic science since 1976. He has testified over 1000 as an expert in drug identification for the prosecution over 1000 times while with the Florida Dept. of Law Enforcement Crime Laborotory. In addition, he was one of ... See full profile

Florida (FL), USA

Expert in Personalized Medicine, Genomics, Proteomics, Bioinformatics, Oncology, Biotechnology, IBD
As the director of the Expert's Firm Genomics and Proteomics Center and of the Dana Farber/ Harvard Cancer Center Proteomics Core, Expert has ample expertise in bioinformatics, since each of these facilities includes a whole ... See full profile

Massachusetts (MA), USA

Expert in Chemical Biology, Medicinal Chemistry, Drug Discovery, Cancer Pharmacology, Hypoxia
A major aspect of Expert's research is focused on how to circumvent or exploit resistance mechanisms by the development of tumour-selective agents targeting abnormal enzymatic expression in cancer tissues. He has had a long-standing interest in certain ... See full profile

United Kingdom

Expert in Pharmaceutical Product Development, Dosage Forms, Controlled Release, QC/QA, GMP, China
Expert has worked in the pharmaceutical industry as a research scientist, QC/QA director, vice president of product development, and has been involved in product development from pre-clinical through Phase 1 production. Expert has experience in setting up ... See full profile

Oklahoma (OK), USA

Expert in Immunology, Pre-clinical Drug Development, Inflammation, Vaccines, Infection
Expert trained in Immunology at the Universities of Birmingham and Bristol in the UK and became Professor of Immunology in 2005. He has particular expertise in cellular immunology, mucosal immunology and infection. He has worked widely with drug ... See full profile

Somerset, United Kingdom

Expert in Human Genetics, Genomics, Genotyping, Realtime QPCR, Sequencing, Forensic, Pop & Statistical
Expert has extensive experience of molecular and human genomic technqiues, DNA extraction, PCR, QPCR, sequencing, forenisc analyses and consulting on design and analysis of genetic disease studies using a range of analytic technqiues. See full profile

LEICS, United Kingdom

Expert in Pharmaceutical Product Development, Analytical Chemistry, Material Science, Process Development
Expert has extensive experience in pharmaceutical product development, particularly in developing drug/medical device combination products. He has over 15 years relevant experience in the pharmaceutical industry, highlighted by the launch of an anticipated ... See full profile

California (CA), USA

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 Genomic Technologies, Bioinformatics, Computational Biology and their Applications
Expert completed is PhD in theoretical physics and two years as a postdoctoral fellow in physics before receiving a five-year fellowship to work on the Human Genome Project. He began working on genome mapping at the Salk Institute in 1992, ... See full profile

Massachusetts (MA), USA

Expert in Neuropharmacology, Intoxication, Drug Abuse, Disability, Poisoning, Pharmacological Pain Management
From a background in behavioural pharmacology of opiate and non-opiate analgesic drug development and cognition-related drug effects, in both university and pharmaceutical industry basic and clinical research, Expert has thirty post-doctoral years of ... See full profile

Tennessee (TN), USA

Expert in Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management
Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, ... See full profile

Maharashtra, India

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