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

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Articles

A technology management process identifies and evaluates new technologies in biopharmaceutical manufacturing to aid business decisions.

Evaluating Technology and Innovation in Biopharmaceutical Manufacturing

Jennifer Markarian is manufacturing reporter for Pharmaceutical Technology.

A Q&A with FDA to gain insight on FDA's views of three-dimensional printing and its regulation in drug manufacturing.

FDA and the Emerging Technology of 3D Printing

PharmTech’s 2016 survey shows general satisfaction with existing solid-dose and parenteral manufacturing equipment, and slow adoption of continuous manufacturing processes.

Measuring Equipment and Manufacturing Trends

An Interview with Aprecia about ZipDose Technology

An MIT-developed system uses microbes for manufacturing small amounts of vaccines and other therapies.

Portable Device Delivers Biopharmaceuticals on Demand

Fintan Weston is manufacturing director at Symbiosis Pharmaceutical Services.

While isolators may offer advantages in high-speed commercial manufacturing lines, RABS continues to be a flexible alternative solution for small-scale production of drugs for clinical use.

Debating the Role of RABS and Isolators in Aseptic Manufacturing

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

Amgen discussed the drug-delivery approaches to two of its biologics in a recent second-quarter earnings call.

Amgen: Neulasta Safe for Now; Dose Accuracy of Erenumab a New Focus

NIST’s monoclonal antibody reference material can be used as a standard for biopharmaceutical analytical quality control.

NIST Issues mAb Reference Standard

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

FDA and industry seek speedy Congressional approval of new user fee plan.

The Industry Hopes Congress Approves PDUFA Program in 2016

The Phase I trial will test Bavarian Nordic’s vaccine, which is manufactured using a vaccine vector based on smallpox.The recent resurgence of yellow fever incidences over the past six months has prompted health officials to ramp up the fight against the virus. Like the Zika virus, yellow fever is transmitted primarily through the bite of infected female Aedes aegypti mosquitoes.