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LATEST CONTENT

Sample Management, Biobanks and Biorepositories do the Definitions Matter?  

The definitions of biobank and biorespository are used interchangeably by some and with exclusive definitions by others. Is it important or does... Learn more »
October 20,2014 by Robert Musterer 

Advancing Information Security and Privacy: The Key Steps in Applying the ISO 27k Framework  

The medical device industry is ever changing and evolving, especially in recent years with adjustments to regulations and the implementation of new... Learn more »
October 17,2014 by Patrick Reichmann 

Mapping the Data Universe: Big Data Presents Big Challenges for the Pharmaceutical Sector  

Adopting a continual, pro-active approach to information governance is essential if pharmaceutical companies are to meet the challenges presented by... Learn more »
October 16,2014 by Martin Bonney 

UPCOMING EVENTS

UPCOMING WEBINARS

  • RBC’s Epigenetics Toolbox: Enabling Epigenetic Research and Drug Discovery Register now »
  • Translational Medicine Informatics - A Biopharma Case Study Watch now »
  • Product Inspection in the Packaging Industry - Are You Ready? Watch now »
  • How do You Maintain a Low Risk Global Supply of Drug Delivery Products in an Ever Changing and Uncertain World? Watch now »
  • Don't Let Geopolitical Developments in Eastern Europe Derail Your Clinical Trials - Applying Local Knowledge Watch now »

LATEST WHITE PAPERS

The Future of Clinical Trial Supply – Trends and Challenges 2015 Report  

To discover the driving trends and priorities in clinical trial supply, Pharma IQ recently conducted the Clinical Trial Supply Outlook Survey 2015. This collected information and opinions from a diverse array of clinical trials professionals to take the pulse of this changing area. In this report, we gather these responses as well as expert insight on the findings along with interviews with thought leaders and articles on key trends to give you an in depth look at the current state of clinical trial supply Read more »
October 14,2014

The Antidote - Taking a Look at Corporate Inversions and e-Health  

Summer is at an end and whilst corporate activity continued apace, including AbbVie acquiring Shire, Omega Pharma attracting acquisition interest, and GSK and Sanofi seeking to dispose of certain of their older drugs, some of you have been cooling off with the ALS Ice Bucket Challenge! This icy event not only brought attention to this rare disease, but highlighted that the drug development pipeline for ALS needed to be bolstered, and reminded us of the high level of costs associated with drug development, particularly if a drug fails. Let’s see whether this innovative, albeit chilly, approach to raise awareness encourages more companies to look to drug development. Read more »
October 10,2014

Trends and Success Factors in Disposable Technologies and Single Use Systems for Biomanufacturing  

Pharma IQ recently conducted their annual online survey looking at the priorities and investment levels of biomanufacturing professionals currently considering single use systems. The 2014 survey gathered the responses of stakeholders from around the world and focuses on their known concerns and challenges, as well as criteria for vendor selection. In this benchmarking survey report Pharma IQ draws comparisons with previous survey conducted at the end of 2013. Find out what has changed since the earlier benchmarking survey conducted in 2013. Read more »
October 10,2014

LATEST INTERVIEWS

Advancing Information Security and Privacy: The Key Steps in Applying the ISO 27k Framework  

The medical device industry is ever changing and evolving, especially in recent years with adjustments to regulations and the implementation of new standards. In this exclusive Pharma IQ interview Patrick Reichmann, Quality Assurance & Regulatory Affairs Manager at Agfa HealthCare, speaks to Pharma IQ about the main challenges being faced by companies in regulatory affairs and what he thinks will be the major trends in the regulatory side of medical device software in the next couple of years. Reichmann also runs through the key steps in applying the ISO 27k framework in order to advance information security and privacy and discusses the importance of safeguarding your existing legacy products. Read more »
October 17,2014 by Patrick Reichmann 

Wide-Scale Adoption of Single Use Systems in Biomanufacturing – The Challenges that Lie Ahead for Suppliers and End Users  

In this exclusive Pharma IQ interview Jerold Martin, Sr. V.P. Global Scientific Affairs, Biopharmaceuticals at Pall Corporation and Chairman of the Board Bio-Process Systems Alliance (BPSA), discusses the growing trends in the single use technology landscape, with a specific focus on the key challenges and opportunities facing countries in the Asian market. Read more »
October 14,2014 by Jerold Martin 

Creating a New Gold Standard Model for Hepatotoxicity - An Interview with David Hay  

Hepatotoxicity becoming apparent in later stages of drug development has cost the pharma industry billions in wasted development costs. A new, reliable, scalable model for liver toxicity is necessary to ensure heptotoxic candidates can be ruled out early. We spoke with David Hay, Principal Investigator at University of Edinburgh’s MRC Centre for Regenerative Medicine about the work currently being carried out with Bristol-Myers Squibb to develop a stem cell derived hepatocyte model. David speaks about how the model matches up with current gold standards and how it can be scaled up for industrial use. Read more »
October 09,2014 by David Hay 

LATEST PODCASTS

Utilising Big Data for Bioscience Product Development  

Big data is turning up everywhere. In this Process Perspectives podcast, Kaare Buch Petersen, Information Architect in Global IT at Christen Hansen, a Denmark-based supplier of bioscience products to food and health industries, talks about how his company has been using big data in the development of their new products. Learn more »
July 03,2014

Fewer Robots, More Apps - An Interview with Jeff Hurst  

The informatics landscape is changing quickly and innovation could be the key to increasing efficiency. Jeff Hurst talks us through these changes and how the industry is moving away from robots towards more innovative methods including mobile apps. He also talks about the dangers of becoming overly 'enamoured with your data' and reinforces that the old rule Garbage in - Garbage Out still applies. Learn more »
March 25,2014

What Pharma can Learn from the Food & Beverage Industry- An Interview with Pepsico's Steve Hills  

The pharma industry has a lot to learn from the food and beverage industry when it comes to contract manufacturing. To get to grips with this outsider's view, we spoke with Steve Hills, European Contract Manufacturing Director at Pepsico. Steve outlines where companies can go wrong in working with CMOs Learn more »
March 13,2014

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