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: 724582 New York, USA

General Hematology/Oncology, Utilization/ Peer-Review, Medico-Legal, Program Develop/Administration

As an academic physician who has extensive experience in research, clinical medicine and administration, he is able to advise on various facets of anticancer drug development and therapy and cytotoxic drug therapy. As an academic physician who has extensive experience…

ID: 724518 Pennsylvania, USA

Business Development and Licensing, Life Sciences

He has broad expertise in the life science industry, ranging from technical and business development of biological and conventional drugs, diagnostics and human nutrition. Expertise involves the use of conventional and molecular diagnostics in disease diagnosis and drug development with…

ID: 724481 United Kingdom

Pharmaceutical Development, CMC, Project Management, Intellectual Property

Expert has developed modified release products throughout his career. Most recently he led the development of proprietary oral modified release systems at Phoqus Pharmaceuticals. These included zero-order, increasing-rate, pulsatile, delayed-release, chronotherapeutic and fast-release formulations. Prior to that he was responsible…

ID: 724265 Canada

Neuropharmacology, Aging, Brain Injury, Memory Impairments, Imaging, Neurodegenerative Disorders

Expert has worked on several projects involving Alzheimer's disease (AD). In particular, he has used genetically engineered mouse models to test ideas and answer questions related to how biological memory might be affected by AD pathophysiology. In addition, he has…

ID: 724240 California, USA

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 supporting approval process. In addition,…

ID: 724018 Massachusetts, USA

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,…

ID: 723580 Netherlands

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…

ID: 723519 Florida, USA

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 support, including analytical method development, process support,…

ID: 723155 Ireland

EU GMP and Quality Systems

Educated to bachelors degree and masters level in biochemistry with many years experience in this field educated to bachelors degree level with many years experience in the field The Client retained Expert of Employer to help and guide it towards…

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…

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