The 2015 CPhI Pharma Awards honors innovation in all phases of small-molecule and large-molecule drug development. Deadline extended to 14 August, 2015. / read more /
Shire takes its offer for an all-stock transaction to combine with Baxalta to shareholders after Baxaltadeclines to discuss the proposal. / read more /
With the product lifecycle moving so fast, many organizations may ask the question, “how can we effectively measure quality?” What can an organization do to keep up with this new pace of business while ensuring the visibility that quality deserves? The answer is Risk Management.
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Peptide quantitative analysis requires workflows that deliver high levels of data quality while balancing the needs of sample throughput and regulatory compliance. Learn how advances in sample preparation can enable greater speed, reproducibility, and improved data quality. Sponsored by: Thermo Fisher Scientific
The new ICH Q3D Guideline for Elemental Impurities has initiated reviews and changes in quality testing programs in bio/pharmaceutical companies around the world. Companies need to assess the risks of potential elemental impurities in their process and materials streams. In this webcast, experts review the requirements of elemental impurities guidelines, practical recommendations to address implementation challenges, and key considerations for analytical testing programs. Sponsored by: SGS Life Science Services
A compilation of articles in a three-handbook set covering general Analytical Testing and Stability in the manufacture, packaging, storing, and testing of formulated products. / Click here /
