Articles by Adeline Siew, PhD - Pharmaceutical Technology

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Articles by Adeline Siew, PhD

Adeline Siew, PhD


Adeline Siew is the editor of Pharmaceutical Technology Europe. Adeline Siew joined the editorial team of Pharmaceutical Technology and BioPharm International in 2012. She has a pharmacy degree from the University of Strathclyde and a PhD in Pharmaceutics (Drug Delivery) from the School of Pharmacy, University of London, where she also did her post doctorate research. She previously worked as an editor at IMS Health and BioMed Central before joining Advanstar's Pharm Sciences group.

Articles
Kickstart Your Experience with the CPhI Pre-Connect Congress
September 15, 2014

An opportunity to broaden your horizon on the latest and hottest industry trends that shape the pharmaceutical landscape.

CPhI Worldwide Returns to Paris
September 15, 2014

The countdown has begun for one of the world?s largest pharmaceutical networking events.

Meeting the Challenges of Excipient Variability
September 1, 2014

The quality and composition of excipients can vary due to environmental factors, processing methods, raw material quality, manufacturing location changes, and even operator actions.

Bioavailability Enhancement with Lipid-Based Drug-Delivery Systems
August 2, 2014

Experts from Capsugel and Catalent discuss the rationale of using lipid-based formulations to improve the oral bioavailability of poorly soluble drugs.

Tracking the Pulse of the Pharmaceutical Industry
August 1, 2014

Pharmaceutical Technology Europe marks its 25th anniversary.

Advances in Controlled-Release Drug Delivery
June 2, 2014

Industry experts share their perspectives on key advances in controlled-release drug delivery and future innovations in this arena.

Freeze Drying Protein Formulations
May 2, 2014

Common challenges and key considerations when developing a freeze-drying cycle for protein pharmaceuticals.

Extractables and Leachables Testing
May 2, 2014

Industry experts discuss how extractables and leachables studies are designed using a risk-based approach.

Navigating the Regulatory Landscape of Combination Products
April 2, 2014

Mark D. Kramer talks about combination products from a regulatory perspective and explains the implications of FDA's final rule on current GMP requirements for combination products.

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