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: 728603 Massachusetts, USA

Chemical and Pharmaceutical Development – Comprehensive CMC

Expert has worked on research, development and manufacturing problems involving stereochemistry throughout his academic training and industrial career. Relevant examples include: development of scalable chiral and asymmetric syntheses; improvement of reaction stereoselectivity; tracking of chiral integrity in chemical processes; chiral…

ID: 728464 New York, USA

Pharmaceutical Chemical Process R&D, Manufacturing, Disaster Recovery, Software Design

As the IT Manager for a major pharmaceutical company Expert has expertise in selection and validation of document management systems, inventory control, instrument calibration systems, as well as computer software utilized in the pharmaceutical industry as a whole. He has…

ID: 728217 Maryland, USA

QC/QA, Sterility Assurance, Aseptic, Pharmaceutical, Biotech, Device Manufacturing & Testing

Environmental Monitoring Operations, EM Trends Reports, EM Remediation and Investigation. Cleanroom Contamination Control Practices, Behaviors, Personnel, Gowning, Cleanroom Traffic Guidelines, Process/Personnel and Product Flows. Microbiology Release Testing-Bioburden, Sterility Test, Growth Promotion, Materials Control, Microbial Identification, Bacteria Endotoxin, Biological Indicators Testing,…

ID: 728090 Switzerland

Pharmaceutical Development, strategy planning and execution

Expert graduated in Biology at the University of Utrecht, The Netherlands, in 1984. From 1985-89 he was a PhD student at the University of Basel. The research in the field of gene regulation was carried out at the Friedrich Miescher…

ID: 726908 New Jersey, USA

Drug and Vaccine Adverse Effects, Standard of Care, Hepatitis

Expert is board certified in internal medicine with a focus on biomedical clinical research. He received his PhD in immunology and medical genetics from the Department of Microbiology at UCLA in 1977. He also received his MD from UCLA in…

ID: 726399 United Kingdom

Aluminium Wire Production and Products

Expert graduated in Metallurgy at the University of Sheffield in England and went on to complete a PhD in the thermodynamics and electrochemistry of high temperature, pseudo refining reactions. His first role in industry required the use of this electrochemical…

ID: 726016 New Jersey, USA

Biotech, Pharma and Medical Device Product and Process Development, Scale-up & Commercialization

His approach to process validation is that PV begins at the process development phase. A process that is well understood, well defined as per the critical to quality attributes with an understanding of the variable interactions prior to the definition…

ID: 726012 Florida, USA

Offshore Oil and Gas Construction Management

Offshore Installation Advisor, Interface and Delivery Coordinator and Offshore Representative with over 47 years of project management experience in offshore construction, fabrication, and marine installation. A US/UK dual citizen resident in London. Offshore credentials include in-date OPITO BOSIET and GOM…

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: 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,…

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