Discover the key technologies, risk mitigation strategies and development considerations shaping modern pharmaceutical formulation — from early-stage selection through to commercial-scale manufacturing.
Successful formulations can enhance the stability, bioavailability and performance of a drug product, while also improving patient usability. The final drug product comprises the active pharmaceutical ingredient (API), excipients and, where applicable, a coating, which can each influence the product’s properties and therapeutic performance. Selecting an appropriate formulation therefore involves multiple steps to ensure it is optimal, scalable and compliant with regulatory requirements.
This report will explore the latest advances in drug formulations, from nanotechnology and lipid delivery systems to bioavailability-enhancing excipients and advancements in lyophilisation. This report will also explore the key challenges in pharmaceutical formulation development, from selecting the most appropriate formulation technologies and identifying risks early in development to ensuring successful scale-up, manufacturing and regulatory compliance. It will also examine the critical role of quality control in delivering robust, commercially viable formulations.
Inside this report you’ll discover:
Download the report to explore some the issues at the forefront of pharmaceutical industry discussions around pharmaceutical formulation from European Pharmaceutical Review >>