Insights On Solid Dose Manufacturing
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NanoImprove The Performance Of Your Formulations
9/24/2024
Learn how Nanoforming can help improve the performance of your molecule by increasing drug loads, improving bioavailability, enhancing drug delivery profiles, and supporting product differentiation.
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Intro To USP <1062> - What It Is And Why You Should Use It
7/20/2023
Knowing how to use USP <1062> helps manufacturers manage the wide variety of factors that can exacerbate production costs, or result in no product at all.
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Optimizing Tablets For Even Splitting: The Pressure Sensitive Bisect Design
11/11/2024
The pressure-sensitive bisect design allows accurate tablet splitting by maximizing facet width, optimizing angles, and balancing radius values for durability and user-friendly administration.
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4 Key Factors To Consider During The Design Process In Aseptic Manufacturing
3/27/2025
From de-risking initial processes to planning full-scale production, crucial decisions shape success. Explore four vital factors that demand careful consideration during the design phase.
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Fundamentals Of Power Blending Simulations
2/26/2025
Predicting blending quality doesn't have to be a guessing game. Learn how to leverage virtual prototypes to make informed decisions and minimize costly trial-and-error in tablet manufacturing.
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Combining Patient Centricity And Commercial Viability In Pediatric Product Development
8/15/2024
Medication acceptance and adherence are critical concerns in pediatric populations due to these patients’ rapid anatomical and physiological development.
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Head Pressure In Your Hopper: What Is It, And How Do You Mitigate It?
7/30/2024
What is head pressure in your hopper and how does it relate to tablet press performance?
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A Micronization Method Enabling The Formulation Of Biopharmaceuticals
6/29/2023
See how applying lyophilization-based micronization methodology at a small scale helps to support challenging formulation development projects.
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Seizing Market Share Pre-Patent Expiry: The Evolution Of A CDMO Partnership In Navigating A Paragraph IV ANDA Submission
6/26/2024
The dynamic pharmaceutical landscape demands agility and strategic foresight. Explore how leveraging a key partnership helped to overcome a looming patent expiry for a second-generation acne medication.
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Closing The Duration Gap In FDA-Approved Long-Acting Contraceptives
7/17/2024
A gap exists between three months and three years in FDA-approved long-acting contraceptives (LACs). A microsphere formulation enables sustained release over a six to twelve-month period.