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As the pharmaceutical industry relies on faster drug development and cost containment to maintain growth, there has never been a more important time to develop strategic CMO alliances to facilitate entry into emerging markets, reduce costs and increase product revenue. But with so many CMOs to choose from, how can you guarantee that you have the right partner to provide the services you require with minimal risk and maximum efficiency?... Full Whitepaper » |
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Breakthroughs in CRO Customer Service Register Now »
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EU Product Launch – Key Considerations for Successful Niche and Orphan Drug Product Launches Watch Now »
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The Changing Face of Sample Management Watch Now »
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From Produce to Patients: Improving Efficiency, Accountability and Accessibility Through Use of GS1 Standards Watch Now »
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Exploring Challenges and Opportunities in Predictive Safety Tools: Trends from Industry-Wide Surveys Watch Now »
- Improving the Security, Quality & Compliance of your Biologic Operation 2/21/2012
- Do’s and Don’ts for Strategic Planning of Laboratory Informatics 2/21/2012
- The Zebrafish (Danio rerio) In Vivo Model for Preclinical Toxicity Testing 2/20/2012
- Implementing QbD Initiatives 2/20/2012
- Survey: Improving Solubility 2012 2/20/2012
- Pharma M&A – Are You Ready For The Next Round? 2/17/2012
Improving the Security, Quality & Compliance of your Biologic Operation
Contributor: Pharma IQPosted: 2/21/2012
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As the distribution of biologics becomes more complex, the associated challenges for compliance, quality and security are likely to increase. Demand for biologics in the United States is expected to exceed $100 billion in 2015. But in meeting this demand, companies are expected to take an increasingly global view. Full Article » |
Valea Video Series - Life Sciences & Chemistry
Contributor: Valea Content SeriesPosted: 1/10/2012
Meet a couple of Valea’s skilled and creative consultants and let them guide you through our offer, acomplete range of IP services. Valea’s team is made of consultants specialising in European patents, trademarks and design, as well as lawyers with specialist knowledge, considerable experience and expertise within all technical areasand legal issues related thereto. Our knowledge is combined with an in-depth understanding of the commercial value of intangible assets to our clients. Full Video » |
Effective Implementations of New CDS Software in FDA Regulated Industries
Contributor: Amber ScorahPosted: 2/16/2012
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Purchasing new software is a significant commercial and resource investment for any level of the pharmaceutical industry. Smooth implementation is essential to minimizing the impact it will have on the organization and internal processes. In this podcast, Prasad Panzade, Director of Analytical Services R&D and QC at Cambridge Major Laboratories, discusses how to effectively manage the challenges that come with software implementation. Full Podcast » |
The Zebrafish (Danio rerio) In Vivo Model for Preclinical Toxicity Testing
Posted: 2/20/2012The zebrafish is emerging as a complement to existing in vitro technologies and established preclinical in vivo models that can be scaled for high throughput. Technological innovation has helped the zebrafish embryo gain ground as a disease model and an assay system for drug screening. Full Whitepaper » |
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13th Annual Lean Six Sigma for Pharmaceutical, Biotech and Medical Device Excellence
February 21-23, 2012,
The Georgian Terrace, Atlanta, GA -
Pharmaceutical Logistics Middle East
February 26-28, 2012,
Amwaj Rotana, Dubai, U.A.E -
4th Annual Disposables Solutions for Biomanufacturing
February 27-29, 2012,
Husa Park President, Brussels, Belgium
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About Pharma IQ
Pharma IQ, a division of IQPC, is an international online community focusing on providing pharmaceutical and biotechnology professionals with knowledge, information and biotechnology articles. We are dedicated to creating a learning environment for sharing ideas, best practices and solutions within the pharmaceutical and biotech community.
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