Tuzistra XR for cough relief is said to be the only twice-daily, extended-release codeine-based cough and cold syrup available in the US. / read more /
Mumbai-based Cipla agreed to acquire US companies InvaGen and Exelan, giving Cipla US tablet and capsule production capacity, a more diversified portfolio, and market access. / read more /
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After many legal proceedings surrounding the first FDA-approved biosimilar, Zarxio was officially launched commercially on 3 September 2015. / read more /
The Fairfield, NJ facility has been upgraded to be Biosafety Level 2 (BSL-2) compliant, according to the Centers for Disease Control and Prevention (CDC) guidelines. / read more /
This agreement follows a collaboration between both parties for the development and manufacture of Lecigon batches for recently completed clinical trial. / read more /
Appropriate cleaning procedures are crucial for any cGMP aseptic or sterile pharmaceutical manufacturing process, including vial filling; operators share best practices for cleaning. / read more /
Agilent Bio-Monolith Protein Affinity columns
Now with two affinity ligands – Protein A and the new Protein G for IgG molecules which have low bonding affinity for Protein A.
• Fast separations to determine titer quickly and accurately on many samples for rapid cell culture development and optimization
• High binding capacity
• Compatibility with a wide range of elution buffers
• Long column life / Read More /
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The biopharmaceutical industry has seen ever increasing innovation over the past five years. Most notably, there has been an increase adoption of high-throughput process development (HTPD) and single-use technologies. Join our webinar to learn effective strategies to match product quality attributes for a biosimilar product and reduce process development timelines. Sponsored by Patheon
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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 /