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: 726895 New York, USA

Maternal-Fetal Medicine

Expert recieved his MD at the University of Michigan Medical School and trained in Obstetrics and Gynecology with a specialty in Maternal-Fetal Medicine in New York. He has been working in the field as an instructor and a medical doctor…

ID: 726774 Illinois, USA

Neuroanesthesia, Neuroprotection, Operating Room Operation & Management, Supply Chain Issues

Expert is board certified in Anesthesiology. After receiving his M.D. degree from Rush Medical College in 1986, he received his training at Washington University School of Medicine with an internship in general medicine in 1987, resident training in anesthesiology in…

ID: 726652 Rhode Island, USA

Psychiatry, Addictive Disease, Public Health, Aviation Psychiatry

Dr. is board certified in general, addiction, and forensic psychiatry by the American Board of Psychiatry & Neurology. Expert received his MD from Mount Sinai School of Medicine in New York in 1988, his Masters in Public Health in Epidemiology…

ID: 726001 Netherlands

Regulatory Affairs and Pricing and Reimbursement-European and Emerging Market

She has advised many International clients with regards to requirements for dossiers as well as routemap for ANDA Procedure in addition to the requirements for DMF dossier as well as routemap for EDQM Certificate of Suitability Procedure. She has worked…

ID: 725868 Montana, USA

Quality Assurance, Regulatory Affairs, Marketing and Business Strategy for Life Sciences Industry

He has performed compliance audits to 21 CFR Part 11. He has developed qualification protocols to test systems compliant with 21 CFR Part 11. He has developed advertising campaigns, written copy for advertisements and managed the creative development of advertisements.…

ID: 725858 India

Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management

Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, projects,…

ID: 725428 India

Pharmaceutical Formulations, Nutraceutical Formulations

Expert is an expert in developing multi-source drug formulations and generic equivalents of innovator products. To date, he has developed and put into the international market more than 100 such products. Consultant to Zim Laboratories Ltd. from 1994 to 2000…

ID: 725332 Pennsylvania, USA

Legacy Application Support: Manage, Measure, Improve Using ITIL V3 Service Management Life Cycle

Exper spent 10 years as Director of MIS for the Revlon Health Care, Pharmaceutical Division and managed all IT activities for 5 companies within the division. Major accomplishments were designing and implementing complex pharmaceutical order processing/distribution system and integrating it…

ID: 725075 Minnesota, USA

Orphan Drugs: FDA/EU/Canada; FDA Approval; Drug Development: CMC, QA, QC, Manufacturing

12 product approvals from FDA including 6 new chemical entities, a 510k device, and three major pharmaceutical efficacy indication supplemental approvals. All received 5-10 years of regulatory exclusivity (Hatch-Waxman, Orphan Drug). These products are generating over $100 million dollars in…

ID: 724825 New Jersey, USA

In-Process Analytical, cGMP Auditing, Polymer Characterization, Analytical Lab Design and Management

Expert has 32 years of industrial analytical chemistry experience. For the last 24 years of that period, he headed the analytical R&D organization of International Specialty Products, a $1.7B specialty chemical company (as of 2007). In his time heading that…

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