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Pharma IQ

Quality Management Systems for the BioPharma Cold Chain

Find out what regulatory inspectors focus on regarding quality, and how to create a good QMS.


Presented By: Mary Mazur-Melnyk
Date: 12 April 2012

Pharma IQ Launches New Reports Resource Centre

Providing new insights into the global pharmaceutical industry...


Presented By: Pharma IQ Reports

Breakthroughs in CRO Customer Service

This webinar will cover how FDA submissions can be simplified by having instant and full access to your data, 24*7 and benefitting from a CRO expertise while protecting your IP.


Presented By: Kelly L. Zaleski & Francois Beill
Date: February 23, 2012, 2:00 PM CET

3 Top Tips for Clinical Trial Supply in India

Gagan Bhradwaj, General Manager-Procurement & Supply Management, Zydus Cadila India, speaks about the main challenges for clinical trial supply in Asia now and how the industry is addressing these challenges throughout the supply chain


Author: Pharma IQ

Using Industry Spending Data to Develop Strategic Marketing

Big Pharma showed an increased need for bio-analytical testing, process optimization, stability storage and testing, cytotoxic projects and toxicology.


Author: Kate Hammeke
Featured Content
Pharma IQ Talking Heads - Global Pharmaceutical Contract Manufacturing Roundtable 2012
Posted: 2/16/2012

Pharma IQ Talking Heads - Global Pharmaceutical Contract Manufacturing Roundtable 2012 -

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 »
Events related to this topic:
On Demand & Upcoming Webinars
  • EU Product Launch – Key Considerations for Successful Niche and Orphan Drug Product Launches Watch Now »
  • From Produce to Patients: Improving Efficiency, Accountability and Accessibility Through Use of GS1 Standards Watch Now »
  • Exploring Challenges and Opportunities in Predictive Safety Tools: Trends from Industry-Wide Surveys Watch Now »
Latest Posts in Pharma IQ
Articles

Improving the Security, Quality & Compliance of your Biologic Operation

Contributor: Pharma IQ
Posted: 2/21/2012

Improving the Security, Quality & Compliance of your Biologic Operation - Pharma IQ

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 »

More Articles
Videos

Valea Video Series - Life Sciences & Chemistry

Contributor: Valea Content Series
Posted: 1/10/2012

Valea Video Series - Life Sciences & Chemistry

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 »

More Videos
Podcasts

Effective Implementations of New CDS Software in FDA Regulated Industries

Contributor: Amber Scorah
Posted: 2/16/2012

Effective Implementations of New CDS Software in FDA Regulated Industries

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 »

More Podcasts
White Papers

The Zebrafish (Danio rerio) In Vivo Model for Preclinical Toxicity Testing

Posted: 2/20/2012

The Zebrafish (Danio rerio) In Vivo Model for Preclinical Toxicity Testing

The 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 »
More Whitepapers

Pharma IQ Advisory Board
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Andrea Charles

Andrea Charles

  
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.

Through Pharma IQ, you will be able to access pharmaceutical information resources such as biotechnology presentations and pharmaceutical podcasts, as well as events such as webinars, seminars and conferences.

By signing up to the Pharma IQ membership, you will gain access to our growing database of multimedia presentations from leading pharma and biotech practitioners, weekly newsletters to keep you updated on latest pharmaceutical content and Pharma IQ members-exclusive discounts on pharmaceutical events that offer solutions to your everyday business problems.

Pharma IQ and IQPC provide useful training courses, conference and expositions for pharmaceutical and biotech executives to network and learn the latest pharma business development and trends occurring in organizations today. Pharma IQ focuses on establishing an interactive experience featuring practical, objective and up-to-date insight from pharma and biotech industry leaders.