This session will identify common challenges faced when outsourcing activities in the Medical Device industry, from the earliest stage of the product development process through to contract manufacturing. Particular challenges recently posed by the pandemic and changing regulatory requirements will be covered with tips provided on how to address these. Recommendations will be given on how to identify potential partners and points to consider for their evaluation and selection. A detailed guide will be laid out on how to conduct meaningful due diligence, contracting and developing a lasting mutually successful commercial partnership all in accordance with quality and regulatory obligations.