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Pharmaceutical Outsourcing
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October 16, 2018
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   Is your API ready for scale-up? What to demand from your CDMO

A CDMO that can optimize your API synthesis process early during technology transfer will reduce the risk of project delay or failure. That will also help your molecule run more efficiently in their plant. And time is money.

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» Industry News
 
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» Featured Articles
The Agility Fallacy
The Agility Fallacy
The pharmaceutical industry has focused considerable effort on increasing organizational agility, particularly in terms of reducing cycle times and getting products to market faster. But too often ... read more »
From Virtual to Real: Physiologically-Based Pharmacokinetic Modeling and Simulation
From Virtual to Real: Physiologically-Based Pharmacokinetic Modeling and Simulation
Modeling and simulation have been used in the pharmaceutical industry for over twenty years and can be advantageous for drug sponsors seeking to improve their drug development process and decision ... read more »
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» Featured Partners
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  Industry-leading Fine Chemistry Services for 40+ Years

With world-class facilities and advanced R&D capabilities, our Fine Chemistry Services team can help with product development at every stage, from contract research through commercial-scale manufacturing. read more »
» Featured Video
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  Watch Video: Interview with Michele Luche from AMRI at AAPS 2016
Watch Video: Interview with Michele Luche from AMRI at AAPS 2016
AMRI is a trusted partner for global contract research, testing and manufacturing services for the biopharmaceutical industry. Our specialized solutions include Drug Discovery, such as medicinal ... read more »
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  Watch Video: Halo Pharma's Full-Range Facility in Montreal, Canada
Watch Video: Halo Pharma's Full-Range Facility in Montreal, Canada
Vice President and General Manager Maryse Laliberte of Halo Pharma talks about their facility and its full range capability including process optimization, validation and a dedicated team to supprt ... read more »

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» Featured Whitepaper
Considerations for Development of a Lyophilized Biosimilar
Considerations for Development of a Lyophilized Biosimilar
The patents for a number of parental biologic formulations are destined to expire in the United States between 2016 and 2027. This provides ... read more »
Process Development for Lyophilized Products
Process Development for Lyophilized Products
Identifying the failure points for a product is a necessary part of product development, and enables the development scientist to design a ... read more »
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| Events
EVENT
  Superbugs & Superdrugs USA
Iselin, NJ –  11/12/2018
To address the ever-growing need of informative and thought-provoking discussions, Superbugs & Superdrugs USA conference will offer a jam-packed ... event details »
EVENT
  DCAT Week ‘19
New York City, NY –  03/18/2019
DCAT Week is the premier business development event for companies engaged in pharmaceutical development and manufacturing and related industries. It ... event details »
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