Intellex Acquires Expert by Big Village

We're thrilled to announce that Intellex has acquired Expert by Big Village, effective March 22, 2024. This strategic move enhances our capabilities and strengthens our commitment to delivering exceptional solutions to our customers.

Stay tuned for more updates on how this acquisition will benefit our clients and experts.

For inquiries or more information, please contact us at info@intellex.com.

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ID: 731774 California, USA

Biotechnology (Immunology/Oncology) – Clinical Pharmacology, Pharmacokinetics/Pharmacodynamics

Expert is an expert in drug discovery and development years of experience in clinical pharmacology, pharmacokinetics and clinical trials of antibodies/antibody drug conjugates Trained in Pharmacokinetics and Pharmaceutical Chemistry, Expert has been working in the leading US biotechnology companies in…

ID: 731747 California, USA

Product Development and Regulatory Approval of In-Vitro Diagnostics and Companion Diagnostics

PhD in Biochemistry, MBA in Business and RAC (US) Certification with 15 years of experience in diagnostic assay and system development at top global in-vitro diagnostic (IVD) companies including Roche, Bio-Rad Labs, Siemens Healthcare Diagnostics and Employer. A proven track…

ID: 731558 Massachusetts, USA

Biochemistry, Drug Development, Antibiotics, Proteins, Medicines, Pathogens, and Pharmaceuticals

Expert serves on the faculty of a University, Department of Chemistry and Chemical Biology. He previously held a senior scientist and lecturer position at ETH Zurich, Switzerland. His interests are at the interface of chemistry and biology, where he is…

ID: 731375 Virginia, USA

Molecular Diagnostics and Clinical Laboratory Medicine

As a board certified clinical molecular geneticist and clinical chemist, Expert directed clinical laboratories engaged in testing human samples for various genetic and immunological disorders.

ID: 731324 Sweden

Drug Discovery & Development, Preclinical Safety Assessment: Toxicology, Pathology & Regulatory affairs

ExpertS. Expert has over 33 years of experience in safety evaluation- Toxicology & Pathology – histopathology slides evaluation, Regulatory, drug discovery & development research, having worked in Switzerland, UK, Sweden and India. He has experience both in the pharmaceutical Industry…

ID: 731256 United Kingdom

Molecular Psychiatry and Neuroscience, Neuropharmacology, Cancer Immunotherapy

Expert has combined his extensive expertise in molecular biology, immunology, molecular neuroscience and psychiatry, and cancer biology to develop a new avenue in the discovery of suitable molecular targets for complex treatment of neurodevelopmental disorders (e.g. ADHD). The new treatment…

ID: 731187 Utah, USA

Implant Reactions, Foreign Body Tumorigenisis, Food Adulteration, Vaccinology

Expert has 40 years of experience as a veterinary pathologist. This includes anatomic pathology, tumor pathology, cytopathology and histopathology. His experience includes all animal species from fish to zoo animals, pets and food animals. He has been involved in research…

ID: 731170 New Jersey, USA

Statistics (Pharmaceuticals (CMC): Design of Experiments, Process Validation, Stability)

After receiving a Expert in statistics, expert has worked in the pharmaceutical industry for over 30 years as a non-clinical statistician applying statistical methodologies, performing data analysis, and interpreting results with scientists in research and development. He collaborated with scientists…

ID: 731004 Canada

Bioscience, Pharma, Biotechnology, Research, Publications, Funding

Expert (President, Employer) is professor and an established researcher with international reputation in cardiovascular disease and diabetes. He is recipient of academic awards from Canadian Diabetes Association, the Province of Ontario, Canadian Institutes of Health Research and Heart & Stroke…

ID: 730734 Florida, USA

Transdermal 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. Designing preclinical, clinical and bioequivalence studies. 2. Filing…

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