Pharmaceuticals & Biotechnology | Pharma & Biotech Resources
Summary: Pharma IQ, a division of IQPC, is an international online community focusing on providing pharmaceutical professionals with knowledge, information and articles. We are dedicated to creating a learning environment for sharing ideas, best practices and solutions within the pharmaceutical community Through Pharma IQ, you will be able to access pharmaceutical information resources such as
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Podcasts:
Rainer Voelksen, Vice-President for International Regulatory Affairs at Edwards Lifesciences, joins Pharma IQ to discuss why standards should have internationally compatible software requirements. He also touches upon the European QM approach, the GHTF project and the International
Chuck Sidebottom, Director, Corporate Standards at Medtronic and Dave Osborn, Manager, International Standards at Philips, join Pharma IQ to discuss the current controversy over the application of risk management under the European Medical Device Directives, how the expectations for risk
Rainer Voelksen, Vice-President for International Regulatory Affairs at Edwards Lifesciences, joins Pharma IQ to discuss why standards should have internationally compatible software requirements. He also touches upon the European QM approach, the GHTF project and the International
Chuck Sidebottom, Director, Corporate Standards at Medtronic and Dave Osborn, Manager, International Standards at Philips, join Pharma IQ to discuss the current controversy over the application of risk management under the European Medical Device Directives, how the expectations for risk
In this interview Kenneth J. Olivier Jr., PhD, Director of Toxicology at Merrimack Pharmaceuticals, speaks to Andrea Charles from Pharma IQ, about w hat trends he is witnessing in the improvement of safety assessments, his top 3 preclinical considerations in the
In this interview Kenneth J. Olivier Jr., PhD, Director of Toxicology at Merrimack Pharmaceuticals, speaks to Andrea Charles from Pharma IQ, about w hat trends he is witnessing in the improvement of safety assessments, his top 3 preclinical considerations in the
With budget cuts hitting hard in the R&D field, it is imperative to validate the worth of predictive methods internally as they continue to facilitate the reduction in late stage drug attrition. But the challenges remain: how do we cost-effectively develop and implement these
With budget cuts hitting hard in the R&D field, it is imperative to validate the worth of predictive methods internally as they continue to facilitate the reduction in late stage drug attrition. But the challenges remain: how do we cost-effectively develop and implement these
What does it take to conduct high quality Paediatric Trials? Legislation for paediatric trials in the US and Europe has been developed and both continenants are beginning to work closer on the harmonisation of regulations. But, there are still different interpretations at to
What does it take to conduct high quality Paediatric Trials? Legislation for paediatric trials in the US and Europe has been developed and both continenants are beginning to work closer on the harmonisation of regulations. But, there are still different interpretations at to
In this interview Jorge I. González Borroto, PhD, Senior Toxicologist, Pharmacology and Safety Department at Ferrer, speaks to Andrea Charles from Pharma IQ, about how the company forms their predictive toxicology strategy and the importance of an early toxicity
In this interview Jorge I. González Borroto, PhD, Senior Toxicologist, Pharmacology and Safety Department at Ferrer, speaks to Andrea Charles from Pharma IQ, about how the company forms their predictive toxicology strategy and the importance of an early toxicity
In this Pharma IQ podcast David Topping, Vice President Global Marketing, Brainloop, and Andrea Charles from Pharma IQ, discuss what is out-licensing and the steps companies need to take to protect their intellectual property. Topping also shares his insights on the specialist
In today's age of electronic communication, the ability to properly protect, monitor and disseminate information being transferred becomes more difficult. In this podcast, Joseph Mariano, a Records System Analyst in the Pharmaceutical Industry, discusses new innovative processes and
In this Pharma IQ podcast David Topping, Vice President Global Marketing, Brainloop, and Andrea Charles from Pharma IQ, discuss what is out-licensing and the steps companies need to take to protect their intellectual property. Topping also shares his insights on the specialist
