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.
![](https://experts.expertengine.com/wp-content/uploads/experts/733446.jpg)
Pharmaceutical Formulation (Tablets, Capsules, Semi-solids, Liquids), QbD, and CMC Regulatory/Risk Assessment Issues
Expert is a Pharmaceutical Formulation Scientist with 25+ years' industry/FDA experience developing and commercializing tablets (fast dissolving, effervescent, chewable, coated), capsules, ODT's, coated beads (i.e., controlled release and taste-masked), topicals (liquids and semi-solids), & CBD/hemp products. He also has experience…
![](https://experts.expertengine.com/wp-content/uploads/experts/739694.jpg)
Pharmaceuticals, Formulation R&D & Oral Solid Dosage Forms
Expert is a Pharmaceutical Formulations Development Scientist, with 6+ years of experience in the pharmaceutical field, specifically with tablet capsules, and solid oral dosage forms. He is familiar with the process analytical technology (PAT) tools, design of experiments, and stability…
![](https://experts.expertengine.com/wp-content/uploads/experts/737899.jpg)
Pharmaceutical Dosage Forms
Expert is the founder and the President and Founder of a pharmaceutical technology company since 1997, and Adjunct Professor of Pharmaceutical Sciences, Faculty of Pharmacy, since 2019. Prior to that he was as a faculty member at the Faculty of…
![](https://experts.expertengine.com/wp-content/uploads/experts/723693.jpg)
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…
![](/wp-content/themes/the-box/images/default_avatar.jpg)
Cosmetic Manufacturing
• Successfully Handled a new range of Ayurvedic Manufacturing Factory from the scratch. Efficiently Managed a Factory with 400 man power. • Managed Five 3rd party manufacturing plants successfully. • Successfully Handled Flavour & Perfume Blending unit. • Setting up…
![](/wp-content/themes/the-box/images/default_avatar.jpg)
Formulation
Pharmaceutical product development, scale-up, commercial manufacturing. Process design, improvements, economic changes. Complex product development, bioavailability, absorption enhancement. Intellectual property analysis and guidelines for alternative strategies. Sourcing, quality, regulatory CMC guidance. Proven track record of 30 years in effective product development…
![](https://experts.expertengine.com/wp-content/uploads/experts/735397.jpg)
Pharmaceutical Development
Expert is a former FDA Review Chemist, with > 39 years of career experience in pharmaceutical R&D, Quality Operations and Regulatory Affairs. For 25+ years as a consultant in his own pharmaceutical development advisory firm, Expert has furnished clients with…
![](/wp-content/themes/the-box/images/default_avatar.jpg)
Pharmaceutics
Expert is a process and chemical engineer with a Bachelor from Univercity Laval in Quebec City. He has more than 15 years experience in engineering, automation, validation of manufacturing equipments, clean utilities, pharmaceutical systems and computer systems (cGMP, GAMP5, CFR-21…
![](/wp-content/themes/the-box/images/default_avatar.jpg)
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…
![](https://experts.expertengine.com/wp-content/uploads/experts/731583.jpg)
Pharmaceutical Development
Expert has over 28 years experience as a pharmaceutical executive managing various aspects of drug product development, including outsourced pharmaceutical manufacturing and broad aspects of the CDMO industry. Previously, Expert was the President of Pharmaceutical Development Services and the Chief…