Articles

Tablet  press  design  innovation  has  traditionally  centered  on  large-scale  production  equipment, however,  there  is  increasing  focus  on  the  smaller-scale,  mid-range  models  that  must  have  the capability to support product development, scale-up, tech transfer, clinical batch manufacturing, small and medium batch production, and continuous manufacturing applications.  This range of capabilities demands unique features and design flexibility.  

Critical Requirements of the Mid Range Table Press

Bioavailability of insoluble compounds is one of the biggest challenges to drug delivery. 
Improving bioavailability is crucial to creating dosage forms that are easy to use and meet demands for patient compliance. 


Screening Permeability in Formulation Selection

This excerpted chapter of a longer book reviews the history of the Food, Drug, and Cosmetics act, including milestones, subsequent laws, and predictions for future laws and regulations; explores the role of Regulatory Affairs in product development; and addresses the importance of a quality management system and organization in bringing products to market.

Regulatory Affairs’ Role in Product Development

The COVID-19 pandemic has forced countless difficult decisions to be made in the face of unprecedented uncertainty. Patients, consumers, and industry professionals alike are looking for guidance, support, and answers. With increased demand on pharmaceutical manufacturers to develop a COVID-19 therapeutic alongside all the existing treatments that are still needed by millions, there follows the growing need for strict quality control processes, and the ability to test and release large volumes of newly manufactured vaccines.

Rely on Data, Not Lore to Meet Rising Demand

This ebooklet offers practical advice on the need for SOPs, how to write them, and what should be included in them.

Seven Essential Elements of SOPs

Plan production automation around audit readiness and regulatory compliance. Understand data integrity considerations, infrastructure components, and new technologies supporting GxP.  


eBook:  Planning Audit-Ready Manufacturing Automation

This whitepaper describes the microencapsulation process of coacervation using both aqueous and solvent pathways, and the many benefits for drug developers.

Expanding Solutions for Challenging APIs Through Coacervation

This whitepaper details how technological advancements by Syntegon and Corning allow for ultra high speed pharmaceutical fill/finish.

How pharma fill/finish is speeding up with innovative glass packaging

A Technical Review of Twin Screw Extrusion Technologies for Life Science Applications

An overview of the various components that go into measuring OEE, and ways product inspection equipment can affect OEE in the pharmaceutical industry.

All Whitepapers