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: 723861 Indiana, USA

Process Automation: Process Control, Computer System Validation, Alarm Management, & Modeling

Expert served for several years as a major pharmaceutical company's chief Quality Assurance GMP/GLP computer validation auditor. He chaired the team that developed the company's first policy and guidelines regarding computer validation,- and served for several years as the company's…

ID: 723840 California, USA

Patent Law, Law, Medical Device Design, Drug & Perishable Material Stability, 510(k) Approvals

Expert's legal practice focuses on intellectual property and patents. He is registered to practice both in California for general legal issues, and nationally for patent issues through the USPTO. In addition to filing and prosecuting patents, he also has experience…

ID: 723733 Texas, USA

SARS-CoV-2 Coronavirus, COVID-19, Sanitization Procedures, Forensic Science, Toxicology, DNA Analysis, Food Poisoning, and Toxic Torts

Expert is a Full Professor of Toxicology and has received grants from NIH in the area of Applied Toxicology. Expert has received grants from NIH in the area of Biotoxicology. Part of his research entails molecular analysis of toxins. Expert…

ID: 723727 Virginia, USA

Quality by Design, Good Laboratory Practices, Intellectual Property Security, ICH and FDA Compliance

As the former CIO of a Fortune 50 product development and commercialization subsidiary, and the executive tasked with building an ISO compliant records management program, Expert has had more than 15 years of experience planning, developing, implementing and then managing…

ID: 723717 Massachusetts, USA

ISO 14001 EMS Implementation, Auditing, and Tailored Training; Integration with GRI Reporting

As a former member of TC 207 and former accredited EMS auditor, as well as an instructor of several accredited ISO 14001 Lead Auditor course providers, he was involved with ISO 14001 since the early 1990's - by way of…

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: 723216 Florida, USA

Intellectual Property Law, Patent Law; Industries: Biotech, Pharmaceutical, Life Sciences

Expert's Ph.D. thesis research concerned the plasma proteins, especially fetuin. He completed postdoctoral research fellowships at Harvard Medical School / NIH (Alzheimer’s disease, tau gene, genomic cloning), Johnson & Johnson (skin diseases, homeobox transcription factors), and Memorial Sloan-Kettering Cancer Center…

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: 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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