Product and Services Finder
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Metrics Inc. is one of the most respected contract pharmaceutical research, development and manufacturing companies in the United States today.
Started as an analytical laboratory in 1994, Metrics has evolved into a full-service provider of quality pharmaceutical formulation development; first-time-in-man (FTIM) formulations; clinical material manufacturing (CTM) for Phase I, II and III trials; commercial manufacturing; and analytical method development and validation services.
Three critical differences set Metrics apart from other CDMOs. One, all clients work directly with a Metrics pharmaceutical or analytical development chemist. Two, projects are expedited quickly and efficiently; they don’t languish in an analytical development queue. Three, Metrics’ quality assurance team is highly experienced, ensuring compliance with all regulatory issues.
Services Offered:
Globally, Metrics provides a broad spectrum of services to support IND, NDA and ANDA submissions to the FDA and worldwide regulatory agencies. Clients range in size from large international to small virtual companies. Services include:
• Pharmaceutical formulation development
• Analytical Method Development and Validation
• First-time-in-man clinical materials
• Clinical Trial Manufacturing
• Commercial Manufacturing
• Stability Storage and Testing
• Raw Materials Testing
• Trace Metals Analysis
• Microbiological Testing
• Potent Product Development
Pharmaceutical formulation development services include: handling insoluble and unstable actives, potent and toxic actives, small molecule delivery. Seamless scale-up to commercial manufacturing, fast track development for phase I –III, instant release and controlled release tableting, capsule filling, over-encapsulation, milling, micronizing, and enteric coating.
Analytical methods development and validation services include: Chromatography (LC and GC), Dissolution (UV and LC finish), Moisture, Particle Size, Ion Chromatography, AA/ICP, FTIR, Titrations, Particulate Matter (HIAC), Cleaning Methods (LC and TOC), LCMS.
Other technical services: first-time-in-man API preparations, potent product development, raw material release, trace element testing, stability storage and testing and routine analysis of dosage forms and drug substances.
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1240 Sugg Pkwy.
Greenville, North Carolina 27834
United States
252-752-3800
2527588522
(Fax)
Sales - General
Jeff Basham
252-752-3800
Company Contacts
Company Website
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Formulation Management
Research Library
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Metrics, Inc
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Joe Cobb and his team used the principles of QbD to improve the robustness of a core tablet for a novel modified release oral solid dosage form.
View the AAPS 2012 poster and watch a short video about how Metrics applies the principles of QbD to solve formulation development issues.
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Metrics, Inc
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Dissolution of a Phosphate Prodrug from Hard Gelatin Capsules: A Case Study Thomas B. Gold, Jennifer G. Warren, and David R. Collier
OBJECTIVE To compare dissolution of a phosphate prodrug from three capsule shell types.
BACKGROUND Clinical studies often include an active comparator (an active control) in the specific study design. The respective design compares the standard therapy ...
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Metrics, Inc
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Detection of Label Photoinitiator in a Potent Product: A Case Study D. Williamson, M. Ruff, K. Rispress, J. Warren, F. Harrington
OBJECTIVE To describe the detection and identification of a benzophenone, used as a bottle label photoinitiator, encountered during routine stability monitoring of a potent drug product utilizing a sensitive analytical method.
BACKGROUND An unidentified peak (UNID) ...
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Formulation Management
Marketing Documents
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Formulation Management
Video
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Metrics, Inc
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See an overview of Metrics' potent products development and manufacturing facility.
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Metrics, Inc
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Meet some of the scientists of Metrics, Inc. a contract manufacturing organization (CMO).
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