Dosage Forms

Pramote Cholayudth previously was the managing director of the Professional Conference Center, Ltd. He currently is a validation consultant to Biolab Co., Ltd., in Thailand. He is the founder and manager of PM consult, cpramote2000@yahoo.com.

Articles

This article discusses the evaluation of paired content uniformity and weight variation data sets using F and T tests to ensure that batches meet compendial requirements.

Justification of Using Weight Variation Instead of Content Uniformity for Release of Relevant OSD Forms

Quotient Sciences’ facility expansion is designed to increase support for fully integrated drug development programs.

Quotient Sciences Expands Formulation Development Capabilities at Nottingham Facility

Webcasts

Webinar Date/Time:  Thu, Oct 27, 2022 11:00 AM EDT

Scaling Up ADC Payloads

Hallie Forcinio is packing editor for Pharmaceutical Technology and Pharmaceutical Technology Europe, editorhal@sbcglobal.net.

Materials enhance sustainability and efficiency. 

New Blister Packaging Options

Manufacturers must consider key components of manufacturing solid versus semi-solid drugs to create a successful end product. 

Considerations for Manufacturing Solid Versus Semi-solid Drugs

Sam Turner is director of Technology and Development at Capcium.

Naresh Talwar, PhD, is director of Product Development at Capcium.

Ajay Pazhayattil*, M.Pharm, DBA, Ajay.Pazhayattil@capcium.com, is vice-president, Scientific and Regulatory Affairs at Capcium.

Advancements in soft capsule technology can enable the development of soft capsule formulations, which are becoming the preferred method of oral administration.

Novel Formulations and Line Extensions with Soft Capsule Technology

This article introduces a control chart technique using F statistic for continued process verification of oral solid dosage forms.

Application of F Charts in Continued Process Verification of OSD Forms

Chris Spivey is the editorial director of 

Creating building blocks for good manufacturing practices is essential.

Building GMPs for Solid Dosage

This article is focused on introducing a control chart technique using relative standard deviation (RSD) statistics (i.e., RSD chart); in other words, a coefficient of variation chart for continued process verification. 

Application of RSD Charts for Content Uniformity Data in Continued Process Verification

Dissolution testing has seen recent trends that have led to increased data integrity solutions as well as an increase in biorelevant testing techniques.

Solid/Semi-Solid Dosage