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Ebook
Advancing Complex Molecules
A start-to-finish guide to develop ability, technology selection, bioavailability enhancement, scale-up & commercial readiness.
Advancing Complex Molecules

Complex molecules can bring poor solubility, limited permeability, high dose requirements and scale-up challenges that complicate the path from early development to commercial manufacturing.

Advancing Complex Molecules takes a start-to-finish look at how sponsors can address those challenges through smarter developability assessment, technology selection and drug product design. Featuring expert perspectives from Serán Bioscience, this eBook explores pharmaceutical classification models, bio-performance modeling, amorphous solid dispersions, precision particle engineering, first-in-human development and the transition to commercial readiness.

Readers will learn how early formulation decisions can improve bioavailability, conserve valuable API, reduce downstream risk, and create a more efficient path from molecule to medicine.

👉Download the eBook to find insights and solutions to formulating hard-to-dissolve drugs.

FEATURES:

Engineering Bioavailability: From Molecule to Medicine

Engineering Bioavailability: From Molecule to Medicine

Why early formulation choices and scalable product design matter when bringing complex oral molecules forward.

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Design for Success

Design for Success

A practical approach to developability and technology selection for complex oral drug products.

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Streamlined Product Development: Leveraging Pharmaceutical Classification Models

Streamlined Product Development: Leveraging Pharmaceutical Classification Models

WHITE PAPER

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Precision Particle Engineering: Driving Bioavailability Through Enhanced ASD Speciation

Precision Particle Engineering: Driving Bioavailability Through Enhanced ASD Speciation

In the competitive landscape of drug development, the ability to deliver poorly soluble compounds effectively is a primary differentiator.

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Discovery Enablement to First-in-Human

Discovery Enablement to First-in-Human

An Advanceable Approach to Rapid Development of Enabled Drug Product.

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Mastering The Transition: Accelerating SDD Programs From Development To Commercial Readiness

Mastering The Transition: Accelerating SDD Programs From Development To Commercial Readiness

In today's accelerated development landscape, the transition from early-stage formulation to commercial manufacturing is the ultimate test of a drug program's viability. 

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Other Available eBooks:

Advancing Small Molecules: Managing Complexity From Development Through Commercialization
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Navigating Complexity in Oral Solid Dose Manufacturing
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Building Stability into Pharma Development
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Manufacturing as Strategy
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Equipment Sourcing & The Circular Advantage In Pharma Manufacturing
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Transforming Complex Small Molecules: Formulation Technologies, Scale-Up, and CDMO Innovation
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