Manufacturing Expert Witnesses in Connecticut

The SEAK Expert Witness Directory contains a comprehensive list of manufacturing expert witnesses who testify, consult and provide litigation support on manufacturing and related issues. Manufacturing expert witnesses and consultants on this page may form expert opinions, draft expert witness reports, and provide expert witness testimony at deposition and trial. The issues and subjects these manufacturing expert witnesses testify regarding may include: 505(b)(2), Active Pharmaceutical Ingredient, Agricultural & Hemp Valuation, Anda, Api, Bla, C Gmp, Chemistry And Manufacturing Controls, Cmc, Construction Equipment Appraisal, Crl, Current Good Manufacturing Practice, Drug Master File, Due Diligence, and Equipment Leasing & Financing Appraisal.

Use the search box above to further refine your search for manufacturing expert witnesses by keyword and state. Attorneys contact the experts directly – with no middleman.

Timothy A Anderson

Chemistry and Manufacturing Controls (CMC), FDA

The AquaMarine Group, Inc.

Redding, Connecticut
Pharmaceutical Regulation, Manufacturing - Current Good Manufacturing Practice, ANDA, cGMP, CMC, Active Pharmaceutical Ingredient, Food and Drug Administration, 505(b)(2), NDA, New Drug Application, NCE, Regulatory compliance, BLA, Drug Master File, Method validation, CRL, Due diligence, FDA, Chemistry and Manufacturing Controls, API, label
Timothy A. Anderson, MS, MBA, is a former FDA Review Chemist with over 43 years of career experience in Pharmaceutical R&D, Quality Operations, and Regulatory Affairs. A uniquely inter-disciplined individual, he melds comprehensive pharmaceutical industrial R&D, business development, QA/QC, and consultancy experiences with formal FDA-tenured regulatory credentials. As a consultant in his own pharmaceutical development advisory firm for over 29 years, Mr. Anderson has furnished clients with services ranging from providing regulatory application filing strategies specialized in Chemistry and Manufacturing Controls (CMC), current Good Manufacturing Practice (cGMP), quality system regulation (QSR) audits for finished dosage, and active pharmaceutical ingredient (API) manufacturing, as well as for device, drug-device combination, and biologic products. Technical and regulatory compliance due diligence services are furnished to institutional investors. Mr. Anderson has contributed to...
Timothy A Anderson - Full Listing and Contact Info

Gregg Dight, ASA

Equipment Appraisal Services

Redding, Connecticut
Appraisal & Valuation, Equipment & Machinery - Tangible Assets Appraisal, Medical and Diagnostic Equipment Valuation, FF&E Appraisal, Construction Equipment Appraisal, Mining Equipment Valuation, Oil & Gas Appraisal, Manufacturing, Agricultural & Hemp Valuation, Transportation & Environmental Valuation, Equipment Leasing & Financing Appraisal
Accredited Senior ASA Appraiser (American Society of Appraisers) since 2002 USPAP Compliant Reports (Uniform Standards of Professional Appraisal Practice) Equipment Leasing & Financing Background
Gregg Dight, ASA - Full Listing and Contact Info
You can also find Manufacturing Expert Witnesses in:
California, Colorado, Connecticut, Georgia, Illinois, Indiana, Kentucky, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, Ohio, Pennsylvania, South Carolina, Texas, and Wisconsin