b'E x e c u t i v eL e a d e r s h i p Te a mPaul McMullin, MIM, MBA Head of Global Sales & MarketingPaul McMullin joined Invivoscribe in 2018 as the Head of Global Sales & Marketing. In this role, he leads Invivoscribes worldwide Sales and Marketing efforts with focus on both Diagnostic and Companion Diagnostics (CDx) Products.These Products are sold in over 100 Countries via a Direct Sales Organization as well as Exclusive Distributors. Mr. McMullin has over 35 years of experience working in the Medical Diagnostics Business. Most of that time has been in the molecularand biotechnology fields. His experience includes numerous positions in Sales and Marketing, establishing Direct Sales, Service and Support companies in Europe and Australia, and managing Distributor Sales in over 55 countries worldwide.He has directly managed employees in Japan, China and most major EU countries.Paul McMullinJason GerholdGlobal Director, Regulatory Affairs/Quality AssuranceJason Gerhold joined Invivoscribe in 2012 and serves as the Global Director of Regulatory, Quality, and Clinical Affairs focusing on developing high quality diagnostics that meet both international pathology needs and support pharma partners drug development programs. He directly manages employees in the US, Japan, and China, and is responsible for worldwide compliance to relevant laws, regulations, and standards. Mr. Gerhold has over 20 years of experience in the biotech industry with biologic therapeutics and diagnostics, including process development, regulatory, quality, and clinical roles. Mr. Gerhold has worked in small, medium and large companies; successfully registering IVD and CDx products in several international markets, developing, improving, and maintaining quality management systems while serving as the management representative to regulatory authorities, and leading clinical teams managing international registrational studies. He is known for building strong rapport with regulators and working well with research and pharma teams resulting in highly successful Jason Gerhold partnerships. He has completed trainings and/or accreditations for ISO 13485 Lead Auditor, Six Sigma Greenbelt, Clinical Trials Administration, Project Management, and CTD writing.Jordan ThornesGlobal Director, Clinical LabsJordan Thornes joined Invivoscribe in 2004 and currently serves as the Global Director of Clinical Labs. In this role, he is responsible for leading Invivoscribes global network of clinical labs, The Laboratory for Personalized Molecular Medicine, (LabPMM). There are currently four such LabPMM facilities which are strategically located globally in San Diego, USA; Hallbergmoos (Munich), Germany; Shanghai, China and Kawasaki (Tokyo), Japan. LabPMM aids patients and pharmaceutical companies worldwide with globally standardized and clinically-actionable diagnostic methods. LabPMM utilizes proprietary biomarkers to select the correct patients and monitor and track their critically important response throughout the courseof their disease. Jordan Thornes10'