As combination products continue to advance healthcare, ensuring compatibility between drug formulations and device components is essential for safety and performance. This webinar provides a focused overview of the key principles behind successful combination product development, emphasizing how drugs and devices interact across the product lifecycle.
Participants will explore critical areas including drug stability in contact with device materials, chemical compatibility and interaction risks, biocompatibility considerations, and microbiological safety. The session will highlight potential risks associated with incompatible components and outline testing strategies used to evaluate and mitigate these challenges.
Attendees will leave with a clear understanding of how to assess compatibility, support regulatory expectations, and ensure consistent product quality. This webinar equips professionals with practical knowledge to design and maintain combination products that deliver safe, reliable, and effective therapeutic outcomes.
Who Should Attend:
- Pharmaceutical drug manufacturers
- Medical device manufacturers
- Packaging, drug compatibility, and quality personnel
- Regulatory affairs
- R&D
- Clinical research, compliance, consulting, drug safety, and validation personnel
