Advancements in personalized medicine and other innovations are transforming the way dosage forms are viewed.

Reshaping Dosage Forms

This study aimed to develop a taste-masked drug resin complex using the ion exchange resin Kyron T-114.

Development of Taste-Masked Oral Dispersible Tablets of Cefpodoxime Proxetil

Novel genetic engineering technologies are transforming the design and manufacture of bispecific antibodies, which are emerging as a promising new class of biologics.

Frontrunners in Bispecific Antibodies

Topic

Articles

As the second part of this series, we look at the importance of ?assessing? the punches and dies to check their condition and how this step may help avoid any problems that may occur during tablet manufacture.

Seven Steps to Solving Tabletting and Tooling Problems---Step 2: Assess

Catalent Pharma Solutions announces additional packaging and storage space for highly potent and cytotocix drugs at Kansas City facility.

Catalent Expands Highly Potent Drug Packaging Capabilities

Capsugel gives lead users access to intrinsically enteric capsule technology and support services.

Capsugel Expands User Program for Enteric Capsule Technology

Jill Wechsler is Pharmaceutical Technology's Washington Editor, jillwechsler7@gmail.com.

Manufacturers face regulatory overhaul, while brand-generic debates escalate over biosimilars and labeling changes.

New Era for Generic Drugs

Cynthia A. Challener is a contributing editor to Pharmaceutical Technology.

The parenteral manufacturing industry is taking action to address particulate contamination issues.

Parenterals, Particulates, and Quality by Design

Jennifer Markarian is manufacturing reporter for Pharmaceutical Technology.

A G-CON, GEA, and Pfizer collaboration developed a PCMM (portable, continuous, miniature, and modular) system to produce oral solid-dosage drugs.

Continuous Solid-Dosage Manufacturing Platform Nears Prototype Installation

Vilayat A. Sayeed is Director, Division of Chemistry III.

This review highlights relevant physicochemical drug properties and formulation design considerations critical to quality and performance of the sublingual tablets.

Considerations in Developing Sublingual Tablets—An Overview

Sean Milmo is a freelance writer based in Essex, UK.

The European Union takes the lead in a global pilot project on the marketing approval of generic medicines, highlighting the challenges of achieving consensus among different nations.

WHO Promotes International Collaboration for Generic Drug Approvals

Randi Hernandez was science editor at Pharmaceutical Technology from September 2014 to May 2017.

Amgen is suing Sandoz over Sandoz's biosimilar application for filgrastim.

First Biosimilar Application Kicks Off Legal Battle

Sigma-Aldrich's custom manufacturing services business unit, SAFC, has launched a new protein quality supplement for biological drug production, including biosimilars.