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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Expert Directory

 

Having an expert witness or consultant at your side can help you navigate complex situations with confidence. These professionals understand your industry and excel at conveying crucial information, whether in a courtroom or a consulting environment. At Intellex, we have experts in over 30,000 areas in our database. We enable you to partner with an individual who has the knowledge, educational background, and relevant experience to support your needs effectively.

Utilize our expert finder tool to handpick the ideal mentor or consultant for your specific application.

ID: 740293 Pennsylvania, USA

Pharmaceuticals & Clinical Development: Drug Development Issues, Vaccines, Infectious Diseases, Pediatrics/Rare Diseases, Immunology, and Neurology

Expert is an accomplished physician executive with over 20 years of experience in clinical development, specializing in infectious diseases, vaccines, pediatrics, neurology, and immunology. With an early career at large pharmaceutical companies like Wyeth/Pfizer and Merck, Expert has accumulated extensive…

ID: 732838 Illinois, USA

Pharmaceutical Discovery and Preclinical Development

SPECIFIC PRODUCTS IVIG (Gammar-P IV ) Rhone Poulenc Rorer Marketed AMP – 579 Rhone Poulenc Rorer Phase II Fenofibrate (TriCor) Abbott in-licensed from Fournier. Over $1 Billion in annual sales. ABT-538/ABT-378 (Kaletra) Abbott over $1 Billion in peak annual sales…

ID: 731580 Pennsylvania, USA

Clinical Development, Safety Reviews, Pharmacovigilance, Pharmacoeconomics

• Employer for preparation for an FDA Advisory Committee regarding review of an NDA. • Design and implementation of Phase I-IV clinical studies • Employer to many large pharmaceutical companies • Employer to Biotechnology companies and CROs • Medical safety…

ID: 730696 Italy

Clinical Development, Regulatory Development

Following more than 25 years in the pharmaceutical industry (Big Pharma, Contract Research Organizations, Small Pharma), Expert has accumulated experience from several hundred clinical studies, primarily in Phase I/Phase II ("First-in-Human", "proof-of-concept") across most therapeutic areas (Metabolic, Infectious, Oncology, Urology,…

ID: 725875 Switzerland

Clinical Development

Expert is a Clinical Development executive with over 18 years of expertise and experience in the pharmaceutical industry. Proven track record of successfully managing large budgets with multiple programs and taking drugs from Phase I to Health Authorities’ approvals. Expertise…

ID: 725066 Florida, USA

Drug & Device Clinical Development, Regulatory Approval, Adverse Reactions, Expert Witness

Clinical Pharmacology is the scientific discipline that brings science to the process of drug development, particularly at the key stage where a molecule of interest becomes a drug candidate. From this point, through the rest of Development, the science of…

ID: 724783 New Jersey, USA

Clinical Development Processes and Clinical Trial Technologies

Expert has worked extensively in bringing technology solutions to solve inherent problems of clinical trial processes. The software products he has worked on ranges from 'electronic data collection' to 'document centric' solutions to reduce overall time it takes to bring…

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: 733995 Canada

Clinical Research, Clinical Trials, Drug Development, Drug Safety, Patient Consenting Process

Experienced clinical research professional with a demonstrated global leadership in the pharmaceutical and medical device industry. Global organization and oversight of clinical research, QA and regulatory strategies. Leadership in new business development (medical device and medical software development quality management,…

ID: 725687 Maryland, USA

Medical Device Business Development, Clinical Trials and Regulatory Strategy, Cardiology, Cardiac Electrophysiology

As a board certified electrophysiologist, Expert has extensive experience implanting and evaluating pacemakers. In addition, she was responsible for regulating pacemakers while at the FDA. Several of her publications are in the area of pacemakers. She is a board certified…

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