08.13.25 -- Our Supplier Failed? Heck No, We Failed Our Supplier!

Join Bend Bioscience for an insightful webinar on controlled release (CR) formulations—designed to optimize drug performance, enhance patient compliance, and reduce dosing frequency. Learn how to streamline CR development using efficient polymer screening methods and real-world case studies. Don’t miss this opportunity to gain actionable strategies and elevate your formulation expertise. Register now! Click here to learn more.

Observe as industry experts discuss some of the challenges in HPAPI drug product manufacturing and highlight essential factors sponsors should consider when evaluating a CDMO partner.

Choosing the right packaging partner for your probiotic may be the most crucial step to ensuring your product is safe and potent when it reaches the consumer.

Autoinjector developers are increasingly addressing the challenges of high viscosity formulations through techniques like those used in developing the ArQ™-Bios platform.

Pharmaceutical firms are increasingly turning to enterprise resource planning (ERP) systems to modernize operations. These platforms unify core functions, including supply chain management, manufacturing, and financial planning and analysis.

Examine how finding alternative solvent approaches could allow for lower volumes of toxic solvents, significantly improving both the environmental and human health implications of new drugs produced.

Discover why a pharmaceutical company facing storage space issues decided to outsource its reference samples to Q1 Scientific, a stability storage service provider, resulting in cost savings.

Review our network's drug product capabilities and innovative business model that does not add additional costs to your project.

Our teams work to deliver fully functional and compliant, mechanical and automated systems to our clients from specification to startup and process optimization.