CBtru® oral drug delivery technology

Formulating a highly lipophilic and poorly soluble crystalline molecule, such as cannabidiol (CBD), can be a complex task. In fact, the oral bioavailability of CBD can be as low as 6% in humans, as a result of incomplete absorption in the gut and significant pre-systemic elimination in the liver. CBtru®, a...

Flavors and taste modulation solutions offer exciting opportunities for developers to enhance drug palatability, improve patient compliance, optimize treatment outcomes, and boost brand value. However, designing effective taste profiles is a complex science. We offer:- A pharma-specific taste portfoli...

High-quality specialty excipient portfolio - including GMP-compliant vitamins and vitamin derivatives, as well as flavors and taste modulators - can provide solutions to help overcome even the most difficult formulation challenges.

TheraPEA™ is a highly biocompatible polymer, proven in ophthalmic, intravascular, and intra-articular applications. This highly degradable polymer enables you to create formulations with near-linear sustained release rates - from weeks to six months-plus - thus unlocking the potential for lower dosing freq...

Our high-quality active pharmaceutical ingredients undergo the strictest quality assurance protocol, and industry-leading GMP-compliant manufacturing practices, aligned with ICH Q7. With an extensive and well-connected global network, we ensure consistency, reliable and sustainable supply across multiple r...

The TheraPEA™ technology is an advanced biodegradable polyester amide platform. Designed for optimal performance, TheraPEA™ Technology delivers consistent near-linear release rates and exceptional processing flexibility. Whether you're seeking controlled release solutions or customizable processing options...

In the following interview, dsm-firmenich shows how they are leading the way in pharmaceutical sustainability by addressing key challenges, aligning with the UN SDGs, and driving innovative solutions to build resilient supply chains and reduce environmental impact.

dsm-firmenich, a leading innovator in health, nutrition, and beauty reveals new clinical data confirming that the bioavailability of cannabidiol (CBD)-based therapies can be enhanced in oral solid dosage forms.

dsm-firmenich launches taste solutions for pharma, enhancing drug palatability and market readiness with expert-backed flavors, maskers, and sensates.

At CPHI Frankfurt we spoke to Anne-Cecile Bayne, Global Science & Innovation Lead Pharma and Medical Nutrition, and Marc Hendriks, Vice President Strategy & Business Development, on their expertise in nitrosamines and business strategy at DSM Biomedical.  

Improving the palatability and acceptance of medication to enhance patient compliance and establish clear product differentiation in an increasingly competitive marketplace. 

From high-quality ingredients to regulatory, quality, and sustainability expert services - count on us to help you better the lives of patients worldwide.

Formulating a highly lipophilic and poorly soluble crystalline molecule, such as cannabidiol (CBD), can be a complex task. In fact, the oral bioavailability of CBD can be as low as 6% in humans, as a result of incomplete absorption in the gut and significant pre-systemic elimination in the liver. This has slowed the development of patient-friendly solid oral dosage forms—until now.CBtru®, an innovative, patent-pending drug delivery solution, is making a new era in drug formulation possible—one that unlocks the true potential of highly lipophilic molecules, like CBD. Enabling optimized bioavailability in solid oral dosage forms is paving the way for more patient-friendly delivery systems, such as tablets and capsules. This will help increase patient convenience and compliance, and elevate patient care worldwide.

In the world of pharmaceuticals, managing the intricacies of regulatory compliance, ensuring ingredient quality, and meeting sustainability targets is a complex task.

Our API portfolio is elevated by Verilege™, a distinct suite of expert services and superior customer care that helps simplify the drug approval process. Driven by continuous improvement, Verilege™ helps you achieve and uphold regulatory and quality compliance, progress towards your sustainability goals, and de-risk your supply chain. The Verilege™ program comes in tiered service levels that adapt to your individual needs. This allows you to focus on what really matters - bringing life-changing and life-saving medicines to market.