Featured Webcasts:
Wednesday, March 31, 2010
11:00 AM ET
Online Course: A New Model for Product Development: Aligning Manufacturing Process Development with Early-Stage Product Development
Process development and procurement questions aren't addressed in the current product-development paradigm until it's too late. By the time process developers, quality assurance professionals, and procurement specialists are brought into product development, they may find themselves saddled with inefficient synthetic pathways and difficult-to-procure materials. Speakers Jennifer Miller, Executive Director of Global R&D at Pfizer, and Hedley Rees, Managing Director at Biotech PharmaFlow, discuss new strategies for streamlining product development and realizing greater efficiencies by realigning functions in pharmaceutical product development.
Wednesday, April 28, 2010
11:00 AM ET
Topical Formulation Development and Screening
In this webcast we will help you understand the routes for drug penetration into human skin and the factors which dictate the penetration potential of a drug. You will learn about in vitro skin penetration models of normal and diseased skin for use in screening topical formulations.
On Demand
Protect IP and Reduce the "Sign and Witness" Burden in Lab Informatics Processes
Protecting the integrity and legally defending the authenticity and ownership of your scientific intellectual property is critical for the bio-pharma industry. To accomplish this, data integrity protection controls, such as trusted timestamping, must be integrated into the data workflow of researchers and scientists, particularly in electronic lab informatics systems. These automated measures also can ease the costly and burdensome task scientists must follow to "sign and witness" volumes of research records, allowing scientists to focus instead on their research.
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