Dosage Forms

Oct 02, 2016
Pharmaceutical Technology
This article will equip the excipient vendor with an understanding of QbD from the perspective of the topical pharmaceutical product manufacturer.
Sep 01, 2016
Pharmaceutical Technology
The authors review the regulatory changes associated with the use of dimethyl sulfoxide in finished pharmaceutical dosage forms.
Sep 01, 2016
Pharmaceutical Technology
By Pharmaceutical Technology Editors
Analytics and science-based approaches are shedding more light on these complex dosage forms, promising to improve process control and product design.
Sep 01, 2016
Pharmaceutical Technology
A study demonstrates the feasibility of a novel solid-dose formulation injection technology to effectively deliver a therapeutic treatment without the aid of a needle.
Jun 08, 2016
Pharmaceutical Technology sat down with Charles N. Kettler, PhD, director of Natoli Scientific, to discuss the Natoli Institute for Industrial Pharmacy at Long Island University.
May 31, 2016
By Pharmaceutical Technology Editors
The agency publishes draft guidance on assessing the adhesion of transdermal delivery systems and topical patches.
May 02, 2016
Pharmaceutical Technology
This article examines using experimental design methods to define different procedures for intermediate bulk container cleaning. The authors have evaluated this new approach, in which a highly soluble, low-dose product and a relatively insoluble high-dose product constituted experimental input variables.
May 02, 2016
Pharmaceutical Technology
Armin Gerhardt, associate professor of Pharmaceutical Science, Concordia University Wisconsin School of Pharmacy, discusses the effects of moisture on product quality and how to achieve good control of moisture during pharmaceutical manufacturing operations.
Apr 02, 2016
Pharmaceutical Technology
Pharmaceutical Technology spoke with FDA to get the agency’s insights on how the industry can ensure quality in solid and semi-solid dosage products.
Apr 02, 2016
Pharmaceutical Technology
Industry experts and FDA’s Office of Pharmaceutical Quality discuss the challenges, trends, and regulations involved in ensuring quality in solid and semi-solid dosage forms.
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