11.14.23 -- Use Procurement To Build Long-Term Supplier Relationships

Learn how this biopharmaceutical research sponsor was able to centralize and digitalize the processes involved in clinical supply production through distribution using GxP inventory.

Learn how the establishment of effective guidelines and standardization relevant to cell therapy development can help to minimize delays and lead to more positive outcomes.

Join patient-centric supply chain expert Marco Hogenboom for a discussion on how to accelerate the delivery of advanced therapies in an unpredictable environment through supply chain customization from clinical to commercialization.

Uncover how a small biotech company was able to resolve critical regulatory CMC deficiencies to meet FDA requirements.

Establishing both the QTPP and CQA for your drug at the beginning of the product life cycle is crucial for a successful GMP manufacturing process.

This article explores how delivering cell and gene therapies to patients requires new levels of agility, flexibility, and innovation in the logistical management of supply. 

Explore how interactive response technology (IRT) can solve some common challenges of manually managed clinical trials and how to find the best IRT solution that meets clinical trial requirements.

This webinar aims to introduce the main regulatory themes, as well as provide a practical insight into converting regulatory theory to practical steps to enable DtP on global studies.