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: 722927 North Carolina, USA

Biomaterials: Biocompatibility, Pathology, Devices

Expert J. 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…

ID: 722849 Oregon, USA

Pharmaceutical Development, Design of Experiments

Expert J. Expert has spent many years applying organic chemistry to solving problems in the fine chemicals and pharmaceutical industry. Expert has been involved for many years in developing chemical processes for the fine chemical and pharmaceutical industries. Expert has…

ID: 722846 California, USA

Stroke, Preclinical Drug Development, Translational Research

Expert A. Expert, PhD. FAHA is the Director of Translational Research at Employer in Los Angeles, California. He is directing the preclinical development of new methods to treat acute ischemic stroke. Expert has expertise in developing small molecules, proteins and…

ID: 722843 Georgia, USA

Drug Delivery Using MEMS, Ultrasound, Electroporation and Other Engineering Technologies

Expert has been the founder of two novel fields of transdermal drug delivery and has led a paradigm shift from chemical to physical methods to enhance skin permeability. He published the first paper establishing electroporation of skin. Using this approach,…

ID: 722788 California, USA

Biotechnological Pharmaceutical Chemical Process Development Design Engineering

Expert has applied his extensive background in chemical engineering in various areas including pharmaceutical process and product development; developing new products for pharmaceutical and consumer industries; process, equipment, and analytical method validation in biotechnology areas; and designing and improving various…

ID: 722777 Argentina

Industrial Automation, Advanced Process Control, Project Management, Applied Mathematics

Expert R. Expert has worked on software development for industrial control analysis and design. He has directed several projects in industrial plant automation. Expert has done and published research on uncertain linear systems described by state space equations. Expert has…

ID: 722747 Washington, USA

Arthritis and Collagen Research

Expert A. Expert has expertise in and has established many animal models of disease at multiple institutions. These include models of human rheumatoid arthritis (RA) such as collagen-induced and adjuvant-induced arthritis in rodents. In addition, he has experience in models…

ID: 722674 Alabama, USA

Developmental and Reproductive Toxicology Study Design, Data Evaluation, and Report Review

Expert (prefers “Expert”) has acquired knowledge and expertise on birth defects in three ways: 1) teaching university courses on human embryology and on causes and manifestations of birth defects; 2) conducting lab animal research; and 3) extensive technical consulting and…

ID: 722626 North Carolina, USA

PK/PD Modeling and Simulation; Nonclinical and Preclinical Statistics; Experimental Design

He managed group of 5 biostatisticians working on Phase I and PK/PD trials. His responsibilities included protocol design, statistical analysis plan writing, specification writing, and delivery of product to customers. He was responsible for meeting all timelines and budgets, assuring…

ID: 722568 Delaware, USA

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 human clinical trials under IND controls. Four of…

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