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: 739593 , USA

Pharmaceutical Manufacturing & Packaging: Sterile Pharmaceuticals, Blow Fill Seal, Liquid Filling, Solids Filling, Facilities & Equipment

Pharmaceutical Industry Expert with over 35 years of experience in all aspects of pharma manufacturing and packaging. He is a leader in manufacturing facilities and equipment, with in-depth knowledge of design, construction, start-up, validation, operations, and maintenance. He is an…

ID: 733424 Pennsylvania, USA

Pharmaceutical Manufacturing Processes, Quality Management, and FDA Interactions

Expert is a consultant to the US FDA for Quality issues associated with the manufacture of pharmaceuticals. Expert is a subject matter expert for the US FDA in Warning Latters and Consent Decree work and data Integrity issues. Expert provides…

ID: 732491 Washington, USA

Pharmaceutical Manufacturing, Combination Products, Medical Devices, and Good Clinical Practices

Expert is a retired Public Health Service (PHS) Officer with 16 years of FDA experience in Pharmaceuticals, Medical Devices, Biologics, and Bioresearch Monitoring. She has held the positions of Investigator, Pre-Approval Manager, Supervisory Investigator, and Foreign Inspection Cadre Member. She…

ID: 731331 Illinois, USA

CGMP,Pharmaceutical Manufacturing and Operational Excellence

Expert has over thirty (30) years of experience in the area of pharmaceutical manufacturing, pharmaceutical research and development, outsourcing, operational excellence and cGMP. Expert has broad ranging experience in pharmaceutical development, manufacturing and outsourcing that includes basic research in the…

ID: 725448 Colorado, USA

Pharmaceutical Facilities, Pharmaceutical Manufacturing Processes, Facility FDA Compliance

In addition to having primary responsibility for numerous pharmaceutical construction projects over the last 15 years, Expert has also held several positions with pharmaceutical and medical device companies where he was responsible for the daily operations of facilities engineering, maintenance,…

ID: 723691 Florida, USA

Pharmaceutical Manufacturing, Research and Development, Education & Training

With over 16 years in pharmaceutical manufacturing and research, Expert specializes in solid and liquid oral dosage forms. His career began in compounding and manufacturing at a university pharmacy, overseeing OTC products and FDA-compliant procedures. He later advanced to managing…

ID: 739165 Georgia, USA

Medical/Pharmaceutical R&D and Manufacturing – New Product Approval and Launch Including FDA, EMA, and Asia

With over 40 years of experience spanning design, manufacturing, R&D, and regulatory compliance, the expert has established a distinguished career in the medical and pharmaceutical industries. Over the past two decades, he has spearheaded numerous successful projects resulting in more…

ID: 723693 Florida, USA

Pharmaceutical Science; Preformulating, Development, Chemistry, Manufacturing & Control (CMC) Issues; Paragraph IV Hatch-Waxman & Canadian Notice of Allegation

As the development of a pharmaceutical reaches Phase 3, prior to submission of an NDA, method validation is required. Validation is a demonstration of optimization. By demonstrating the capacity of a method within the bounds of validation, optimal conditions for…

ID: 735625 South Carolina, USA

Pharmaceutical and Fine Chemicals, Small and Large Scale Manufacturing

I earned my PhD at the Technical University (TU) of Karlsruhe, Germany in Organic Chemistry. I have knowledge and experience in the following realms: - Phospholipids - Pharmaceuticals (R&D, Manufacturing) - Vitamins. Highly motivated, results oriented professional with over 35…

ID: 733859 Arizona, USA

Manufacturing Technologies for Pharmaceuticals, Biologicals, Biotech and Vaccines

Expert is an independent consultant to bio-pharmaceutical, medical device and vaccine manufacturers, associated equipment suppliers and investors, with over 40 years experience in aseptic process technology, new product and business development, marketing strategy and regulatory compliance for manufacturing of pharmaceuticals…

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