- Sponsored Content
Rapid Help for Cancer Patients: Fully Integrated Project Solution for Accelerated Supply of Valuable Active Agents to the Market
August 1, 2019
1 Min Read
Sponsored by Zeta Pharmaceuticals
The development of a new, innovative drug is a highly complex and cost-intensive technical task. It normally takes more than 10 years from initial idea to first approval of a drug. As the statutory requirements for patient safety have become ever more stringent in recent years, development expenditure has increased significantly. High investment costs needed to develop some drug products are estimated to be 1–1.6 billion US dollars, which can be amortized only after market launch (1). The race against time for patients and valuable new active agents begins long before a new drug can be
used to save lives.
Given the time pressure to achieve rapid market launch of a drug, innovative solutions are called for to reduce project lead times and to meet ever-increasing quality requirements. The scale-up process for producing active pharmaceutical ingredients (APIs) requires a wide range of outstanding engineering skills, all of which ZETA can
provide optimally by means of system-controlled knowledge transfer. ZETA supplies solutions along the entire API production process. The company proved its expertise recently with a new, integrated, software-based process planning tool that reduces project lead times by 30%.
Fill out the form below to read the complete capabilities review now.
1 The Current State of Innovation in the Pharmaceuticals Industry. CRA International: London, 2008.
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Mar 11 - Mar 14, 2024
Mar 11 - Mar 14, 2024
Accelerate speed to market for your next generation mAbs, vaccines, cell therapy, and gene therapy products. At the BioProcess International US West event in San Diego, CA, in March 2024 you can access today's innovative strategies and technologies designed to improve process efficiencies and maintain product quality across all phases of bioprocessing.Agenda