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.

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.

Extractables and Leachables Testing
May 2, 2014

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

Freeze Drying Protein Formulations
May 2, 2014

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

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.

Tackling challenges in the development of fixed-dose combinations
April 2, 2014

Anil Kane from Patheon spoke to Pharmaceutical Technology about the challenges in the development of FDCs and discussed how to integrate quality-by-design (QbD) in the manufacturing process of FDCs.

Current issues with nanomedicines
March 2, 2014

Despite the progress made in nanomedicine development, there are several issues that remain unresolved. Raj Bawa, PhD, provides insight.

Characterization of nanomedicines
March 2, 2014

Nanomedicines can offer promising benefits in the diagnosis and treatment of diseases but there are still concerns about the safety and quality of these therapeutics partly because of the lack of clear regulatory guidance. Scott McNeil, PhD, director of the Nanotechnology Characterization Laboratory (NCL), spoke with Pharmaceutical Technology about nanomedicine characterization.


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