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501 5th Street , Bristol, TN, 37620, US
Will direct team of formulation scientists who develop oral solid dose formulations for Phase I through Phase III clinical trials.
By: Tim Wright
Frank Sorce brings 30 years of experience in pharmaceutical sales, marketing and business development having held senior sales leadership positions
By: Kristin Brooks
Dr. Chi-Chang Wung joins the company with more than two decades of industry experience
By: Betsy Louda
Dixon to oversee Analytical Testing & Development groups and Microbiological & Raw Material Testing Labs
Curtin was promoted from his previous role as executive vice president of Quality Operations
Anticipates having all of its clients' products serialized by the November 2017 deadline
Bristol facility grows from a $25 hand-operated tablet machine to a 500,000 square-foot campus
Pharmaceutical and biopharmaceutical companies large and small are increasingly relying on third-party providers for support at all stages of drug development. To realize efficiencies, they are at the same time reducing the number of suppliers to a preferred few with whom they can form strategic partnerships.
By: James E.
CMOs, CDMOs and CROs are becoming more specialized to stand out in a hyper competitive market
Comparing manufacturing methods for one immediate-release low-dose form, we found that dry blend needed less equipment and was more “QbD-ready” than wet granulation or geometric dilution.
By: Julie Kuriakose
Meeting the solubility challenge
By: david b hedden
Former King facility moves to CMO
By: Gil Roth
Adds TA Instruments
Will add Xcelodose, bump up manufacturing space by 50%
FDA recommended approval to CDER for UPM to manufacture a low-dose tablet product
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