Universal Regulatory, Inc provides consulting services in Regulatory Affairs, Regulatory Operations, CMC, Medical Writing, combining strong technical expertise in pharmaceutical development with knowledge of global regulatory environments. Founded in 2009, we have a successful track record, having worked with >50 pharmaceutical and biotechnology companies. Universal has established partnerships with consulting firms in EU, Japan, and Asia to be able to support client needs for a global development program. We’re looking forward to working with you through your regulatory and product development life cycle. For more information on how we can support you please contact: Deepa Deshpande, PhD, RAC Email: [email protected] Tel: 510-396-8461 Thank you for your interest and we look forward to connecting with you soon.