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HEALTHPAYERINTELLIGENCE

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Follow BEST Practices When Selecting a CDMO for Drug Formulation
Pharmaceutical and biotech companies evaluating contract development and manufacturing organizations (CDMOs) for formulation development of...

First in Man Oral and Parenteral Dosage Forms
LEARN MORE LEARN MORE LEARN MORE LEARN MORE LEARN MORE LEARN MORE LEARN MORE Formulations for Poorly Soluble & Low Bioavailability Drugs LEARN...

Ascendia Joins the Fight Against COVID-19
Ascendia Pharmaceuticals is proud to announce that it is engaged in multiple collaborations to develop and prepare injectable, inhalation, and...

DOSAGE FORM DEVELOPMENT
The selection of a final dosage form is driven by the project’s commercial needs, and properties of the drug substance. Ascendia offers a range...

Pharm Tech Features Ascendia in Feature on Formulation Trends
Ascendia Founder and CEO Jim Huang, Ph.D. was quoted in a new feature article on formulation trends published by Pharm Tech. The article,...

FORMULATION FORUM: Design & Development of Lipid-Filled Delivery Systems
With increased water-insoluble (BCS II/IV) or low permeable (BCS III/IV) new therapeutic entities filling drug pipelines, lipid-based drug...

FORMULATION FORUM: How Poorly Water Soluble APIs Present 505(B)(2) Opportunity
More than half of all approved drugs on the market contain poorly water soluble APIs. In this Formulation Forum, Ascendia CEO Jim Huang, PhD,...

How to Select a CDMO to Improve Drug Bioavailability and Solubility
Low aqueous solubility is one major problem associated with formulation development of new chemical entities, as well as for generic drug...

State of CDMO Market: Insight From Ascendia
Contract development and manufacturing organizations (CDMOs) are focusing on providing more specialized services. That is one trend Ascendia CEO...

Benefits of Lipid-Based Delivery Systems in Poorly Soluble Drugs
A growing number of pharmaceutical companies’ drug pipelines are being filled with water-insoluble (BCS II/IV) or low permeable (BCS III/IV)...