Grant Senner, MD, DABRM
Chief Executive Officer
Dr. Grant Senner, MD, DABRM is a tested physician executive and entrepreneur with over twenty years of corporate, legal, regulatory and medical finance expertise within the life science and healthcare sectors. He brings progressive healthcare leadership experience with proven success in achieving strategic, operational and financial objectives. His diverse background includes expertise in biomedical technology and commercialization, health finance, clinical program development, medical reimbursement and population health management spanning the commercial and academic sectors.
Upon completion of his Doctorate, Dr. Senner served as Fellow and Consultant for the state of Arizona’s Medicaid agency where he focused on Centers for Medicare and Medicaid Services (CMS) reimbursement models and coordination of care for individuals with complex needs in a patient-centered model. Subsequently, he held key leadership positions within community-based medical practice and biomedical technology companies. In 2012, he joined University of Arizona Health Sciences, University of Arizona, as Director of Special Projects and Strategic Initiatives and was responsible for analysis of market opportunities and support of grant and contract development. Currently, Dr. Senner serves as founder and CEO of several companies focused on regenerative human and veterinary science, including Equus Innovations (Phoenix, AZ) which manufactures the RenoVō ® equine allograft.
An Honors graduate of the University of Arizona with a Bachelor of Science in Molecular and Cellular Biology, Dr. Senner attended the University of Arizona College of Medicine – Tucson and graduated with his Doctorate of Medicine in 2004. In 2014, his family established the Senner Endowment for Precision Health within University of Arizona Health Sciences, dedicated to support the use of genetic profiles to guide the diagnosis, prediction, treatment and prevention of disease.
Ann Kolesar, MBA
Senior Director of Quality & Compliance
Ann Kolesar, MBA, is a seasoned Quality professional, with nearly 30 years experience in FDA regulated industries. She brings extensive knowledge of manufacturing and aseptic processing in pharmaceutical, medical device, biologic, and tissue bank environments, and her diverse background includes expertise in Quality Operations and International Regulatory Compliance (US, EU, CAN).
After beginning her career in the production of aseptic pharmaceuticals, Ann has held numerous leadership positions to include oversight of Quality Assurance, Quality Control, Quality Engineering, Quality Compliance, and Regulatory Affairs. Experience includes direct oversight of Manufacturing and/or Quality (US and OUS) for a variety of dosage forms to include human parental, oral solid, and topical pharmaceuticals, Class III medical devices including combination products, HCT/Ps and veterinary products, in traditional manufacturing, contract manufacturing and virtual environments. Development and management of Quality Systems includes 21 CFR parts 210, 211, 820, 600, 11, 1271; EU MDD 93/42/EEC (2007/47/EC); Ca. C.R.C, c. 870 and SOR/2003-196; AATB; and ISO 13485, 14971 and 9001. Regulatory and Grant submissions include DMF, (Ca) PLA and CTA, IND, ISO 13485 and SBIR.
A proven, cross-functional leader, Ann has consistently met the challenges facing corporate, small business, and start-up companies, utilizing creative approaches and risk-based strategies to achieve compliance objectives while actively managing budget impact. Currently, she serves as the Sr. Director Quality & Compliance for Equus Innovations (Phoenix, Arizona), the manufacturer of the RenoVō® equine allograft.
Ann holds a Bachelor of Science in Biology from Arizona State University and a Master of Business Administration from the University of Phoenix.