Drug Delivery Systems and Quality Assurance

Publications Presentations

Patent Preparation Expert Witness

New Product Acquisition Drug Delivery Systems

Preformulation Formulation and Process Design Analytical Method Development and Validation Feasibility and Stability Quality By Design IND CMC Documentation Bioavailability Reverse Engineering of Pharmaceucial Formulation

Quality By Design Process Optimization Scale-Up and Clinical Manufacture Analytical Methods Regulatory Stability Process Validation Technical Transfer Bioequivalence Testing NDA CMC Documentation

Quality By Design for Excipients Excipient Safety Regulatory Alternate Sources Quality Management Systems

Excipients Drug Delivery Systems Clinical Trial Supplies Medicinal Products

Medicinal drug development is a complex interweaving of many different activities over and extended period of time. Quality Assurance aspects of drug development include excipients, APIs and medicinal products (GMPs), clinical trials (cGMP) and safety testing (GLP).

FinnBrit Consulting can advise clients on the application of GMPs during drug development.

All information published throughout www.finnbrit.com is intended for information only, and does not contain any warranties, implied or otherwise.

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