Katherine Leibowitz is a lawyer who has been supporting the clinical trials enterprise for almost 25 years.  She co-founded Leibowitz Law eleven years ago, after 17 years at a top ten global law firm.  Clients of her boutique regulatory and technology transactional law firm include sponsors, research institutions, technology service providers and CROs.  Katherine’s niche practice focuses on clinical trials and technology commercialization.  She handles the clinical trial operations contracting process from start to finish.  Leibowitz Law combines clinical research (CTA, budget, ICF, vendor MSAs, DMCs and more), regulatory compliance (FDA, fraud and abuse, HIPAA), technology & data (licensing, ownership, cybersecurity, data rights), and corporate & commercial services (risk mitigation, general contract law) to create a cohesive whole.  Katherine is a frequent speaker and author, and enjoys combining the multiple regulatory, legal and industry norms to provide integrated guidance for the life sciences community.