Bringing a drug from discovery to market is an expensive and time-consuming business. Every drug that fails comes with a cost which could be both reputational and financial. Keeping your development program on track is therefore critical to success.

In this presentation, the last in a 4-part webinar series examining supplier quality management for the pharmaceutical and medical device industries, the featured speaker will explore the technology options for managing a supplier quality management program within a centralized cloud-based network that supports all supplier-related procedures and processes.

Following on from the second webinar in this 4-part series, "Quality In, Quality Out: Regulatory Drivers of Supplier Quality Management in the Medical Device Industry," this third presentation will take a specific and deeper dive into the regulatory requirements for supplier management for the pharmaceutical and biopharma industries.

Pharmaceutical development is inherently risky. To develop a molecule that has a desired, efficacious, but safe, effect in humans is a remarkable achievement considering the statistics.

Interest in the medical use of cannabis and cannabinoids continues to grow as patients and caregivers consider this option for treatment of unmet medical needs. Ever growing efforts to legalize cannabinoids in the US and Canada are creating an increased need to evaluate safe and effective use.

Systech International, a global leader in brand protection technologies, will now offer its UniSolveTM serialization software as an integrated solution with labeling hardware from Etipack, a manufacturer of labeling and coding since 1978.