is a Food and Drug Administration inspected sterile liquid fill manufacturer that maintains a tradition of quality and core competency in both current Good Manufacturing Practices (cGMP) and International Organization for Standardization Quality Systems (ISO 9001:2008), representing a unique combination for any pharmaceutical manufacturer. McGuff Pharmaceuticals develops, registers and manufactures brand and generic drug products under its own label, as well as private labels, for distribution to key market segments. McGuff Pharmaceuticals is also uniquely positioned to assist clinical investigators perform phase I, II and III clinical trials. We employ Pharmacists, Engineers, Quality Control, Regulatory Affairs and other personnel that have experience manufacturing, labeling, and distributing clinical trial materials. Our staff provides customers with a wide variety of additional knowledge incorporating current experiences working in hospitals, community pharmacy settings, chemical industry, and commercial pharmaceutical manufacturing. Additionally, we are an experienced pharmaceutical contract manufacturer. Contract manufacturing offers the opportunity for sponsor companies to focus on their core strengths while leveraging our cGMP compliant and ISO certified facilities and regulatory expertise. We offer a defined approach to program management, that offers a variety of technical services to our customers including R&D, product development, product stability, product formulation, and regulatory compliance. McGuff Pharmaceuticals is uniquely organized for our customers with cGMP pharmaceutical contract manufacturing facilities, innovative leadership and a corporate-wide commitment to the highest standards of quality and customer service. We should be your choice as a preferred partner in providing quality, cost-effective health care solutions for your NDA clinical trial and pharmaceutical contract manufacturing needs.
