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February 26, 2019
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   Ajinomoto Bio-Pharma Services, A Fully Integrated CDMO

Ajinomoto Bio-Pharma Services offers comprehensive capabilities for small molecule APIs and biologics production, from process development and cGMP manufacturing to aseptic fill finish, including cytotoxics. As a global CDMO, we provide the adaptive solutions, responsive service, trusted partnership and peace of mind you’ve come to rely on.

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» Industry News
 
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» Featured Articles
Selecting and Qualifying a Regenerative Medicine CMO
Selecting and Qualifying a Regenerative Medicine CMO
Among the most remarkable technical advances seen within the healthcare sector over the last decade is the fast growing sector of regenerative medicine. Breakthrough technologies are empowering re- ... read more »
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 »
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» Featured Announcements
[Webinar] Novel ADC Conjugates: Characterization Tools and Formulation/Process Development
Date: Thursday, February 28, 2019, Time: 01:00 PM Eastern Standard Time
Antibody-drug conjugates (ADCs) are a novel class of drugs that combine the potency of small ... read more »
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» Featured Video
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  Watch Video: Mark Egerton, CEO of Quotient Sciences, Interview at AAPS 2017
Mark Egerton, CEO of Quotient Sciences, Interview at AAPS 2017
Quotient Sciences is dedicated to accelerating the development of new drugs for patients around the world. We provide formulation development, clinical pharmacology trials, and clinical and commercial... read more »
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  Watch Video: Pfanstiehl - Global Leader in Bioprocessing Solutions
Watch Video: Pfanstiehl - Global Leader in Bioprocessing Solutions
Pfanstiehl specializes in isolation, purification, custom synthesis and scale-up development of regulated, high purity and low endotoxin Injectable Formulation Ingredients, Pharmaceutical ... 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 »
Vcaps Plus Capsules
Vcaps Plus Capsules
Hypromellose (HPMC) capsules were originally formulated with a secondary gelling agent. This agent can delay dissolution in some circumstances and ... read more »
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| Events
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 »
EVENT
  SMi’s 2nd Annual Pharmaceutical Microbiology East Coast Conference
Boston, MA –  04/10/2019
The pharmaceutical microbiology industry has seen many changes during the progression into the 21st century. With advances in rapid microbiological ... event details »
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