Dr. Dhillon is an advisor to Arch Therapeutics. He previously served as Chairman of the Board of Directors of Arch from April 2013 to July 2018. He has more than 25 years of experience in building public life science companies organically and through mergers and acquisitions, leading innovation in scientific, engineering and agricultural enterprises, securing significant United States government grants and NGO funding, raising significant investment proceeds from US, Canadian, European and Asian institutions and high net worth individuals, and building dominant IP portfolios through partnering and negotiating transactions with small businesses and large multibillion dollar companies. Dr. Dhillon is a successful executive and entrepreneur who has been instrumental in founding, helping develop and leading a number of companies including, Inovio Pharmaceuticals (NASDAQ: INO), which develops next-generation DNA based vaccines, where he was President and Chief Executive Officer from October 2001 to June 2009, Executive Chairman from June 2009 to August 2011, and Chairman since September 2011; OncoSec Biomedical (NASDAQ: ONCS), which develops DNA-based intratumoral cancer immunotherapies, where he has been Chairman of the Board since inception in 2011; Vitality Biopharma (OTCQB: VBIO), where he served as Chairman of the Board since January 2012; and Emerald Health Therapeutics (TSX.V: EMH), where he has been Chairman of the Board since April 2015.

Previously, Dr. Dhillon was vice president of MDS Capital Corp., one of North America's leading healthcare venture capital organizations. He completed B.Sc. (Honors) and M.D. degrees at the University of British Columbia and practiced family medicine for 12 years from June 1989 to December 2001.

Dr. Ellis-Behnke is the inventing cofounder and a scientific advisor to Arch Therapeutics. His discovery of the immediate hemostasis technology while he was at MIT led to the founding of the company. He holds 10 U.S. patents for multiple discoveries that use nanotechnology to help repair the body, ranging from immediate hemostasis; repairing the optic nerve and demonstrating the reversal of blindness; preserving stem cells; and immobilizing cancer stem cells. Dr. Ellis-Behnke holds affiliate faculty positions at MIT and the University of South Florida Morgani College of Medicine. From 2010 to 2015 he was Director of the Nanotechnology Translational Think Tank in the Mannheim Medical Faculty of the University of Heidelberg in Germany; from 2004 to 2010 he was in the Faculty of Medicine at the University of Hong Kong first as a Research Associate from 2004 to 2006, then as Associate Professor and concurrently Associate Director of the Technology Transfer Office from 2007 to 2010. Prior to returning to MIT to pursue his PhD in 1998, he held various management positions including Senior Vice President of Huntingdon, a public company for pharmaceutical testing and consulting services. In 1995, he became co-founder/CEO of one of the first internet companies in the world to do online commerce. Dr. Ellis-Behnke received his PhD from MIT in Neuroscience in 2003; his BS from Rutgers in Agricultural Sciences in 1984 and a diploma from Harvard Business School’s Advanced Manager’s Program in 1995. From 2006 to 2015 he was the Associate Editor/Neurology for Nanomedicine: Nanotechnology, Biology & Medicine. He is a member of the National Academy of Inventers and a life member of the International Society of Nanomedicine.

John Richards, DPhil., who started advising Arch Therapeutics in 2016, brings over 30 years of pharmaceutical industry and peptide chemistry experience. Since 2009, he has been Vice President of Global Pharmaceutical Development at The Medicines Company, responsible for CMC development and manufacturing of all the company’s products, including the very large scale program for the peptide-based anticoagulant, Angiomax®. He has extensive experience leading CMC programs which have resulted in the successful filing and approval of drugs and biologics in the United States, European Union and other territories.

Previous roles included Director of Process Development at ImmuLogic Pharmaceutical Corporation, where he was responsible for the design, construction and operation of a multi-train peptide manufacturing facility, and Manager of Peptide Synthesis at UK start-up Cambridge Research Biochemicals and its acquirer ICI Pharmaceuticals, where he contributed to pioneering activities in the 1980's to manufacture cGMP peptides at contract manufacturers for pharmaceutical use. 

He earned his doctorate developing protecting groups for use in peptide synthesis at The University of Oxford. While performing his Post-Doctoral work in the Laboratory of Molecular Biology, Cambridge, UK, he was a member of Dr. Robert Sheppard's team that developed the Fmoc-solid phase method of peptide synthesis.

Robert M. Williams, PhD, an advisor to Arch since 2010, is a University Distinguished Professor at Colorado State University. Dr. Williams earned his B.A. degree in Chemistry from Syracuse University in 1975 and obtained his PhD degree in 1979 from MIT. He was a post-doctoral fellow at Harvard University (1979-80) prior to joining the faculty at Colorado State University in 1980 and is now a University Distinguished Professor. He has been a visiting Professor at the University of California, Berkeley (1990) and Harvard University (1994-95). Dr. Williams' research interests utilize the tools of organic synthesis to study problems in chemical biology and medicinal chemistry. Williams has judiciously deployed total synthesis to interrogate hypotheses concerning the biomechanism and/or biosynthesis of complex, biologically significant natural products. Much of Williams' recent work on complex alkaloid and peptide synthesis is based on his development of a practical and commercialized technology for the asymmetric synthesis of a-amino acids, peptide isosteres, peptides and depsipeptides. Dr. Williams has received several Honors and Awards including the NIH Research Career Development Award, The Eli Lilly Young Investigator Award, Fellow of the Alfred P. Sloan Foundation, the Merck, Academic Development Award, the Japanese Society for the Promotion of Science Fellowship, the ACS Arthur C. Cope Scholar Award and the ACS Ernest Guenther Award in the Chemistry of Natural Products. He serves on the Editorial Board of Chemistry & Biology; served as Editor for the journal Amino Acids (1991~1998) and is a Series co-Editor for The Organic Chemistry Series, (Elsevier). Dr. Williams has been a Founding Scientist for several biopharmaceutical companies including Microcide Pharmaceuticals, Xcyte Therapies, HemaQuest Therapeutics, Cetya Therapeutics and Sapientia Therapeutics.

Roger Gregory, PhD, Professor of Chemistry and Biochemistry, Kent State University, has been working with Arch Therapeutics since late 2011. He has provided expertise in product formulation and the relationship between the structure and properties of peptides. Dr. Gregory is a physical biochemist with over 30 years of experience in protein chemistry and analysis. His research interests include protein dynamics, protein hydration, and protein-solvent interactions. He recently returned to the Kent State faculty after serving over seven years as Chair of the Department of Chemistry. As Chair, he helped establish core facilities in genomics, proteomics, bioimaging and 3D visualization. Dr. Gregory earned his BSc and PhD in Biochemistry from the University of Sheffield, England, and performed his postdoctoral work in Protein Chemistry at the University of Minnesota.

Dr. Denman started advising Arch Therapeutics in 2012. He is a Massachusetts General Hospital Anesthesiologist, Clinical Trial Investigator and past Chief Medical Officer of Covidien and GE Healthcare.

Dr. Denman received his medical training in the United Kingdom, completing residency at St. Bartholomew’s Hospital in London, followed by a fellowship at Massachusetts General Hospital, remaining on staff. In 2000 he became Chief of Pediatric Anesthesia at the Floating Hospital for Children in Boston. During his full-time medical practice he was involved in multiple clinical trials and development of pharmaceuticals and devices. He filed and was awarded several patents while focusing on solutions for unmet clinical needs.

In 2003, he began his career at Tyco Healthcare, now Covidien, becoming the Chief Medical Officer and VP for Medical Affairs in 2007. He guided development and implementation of the medical functions throughout Covidien, built a medical affairs, clinical affairs, healthcare economics and reimbursement team; focused these functions on ensuring compliance with new regulations and driving the medical voice into all aspects of the business. From 2010 to 2012, he was the Chief Medical Officer at GE Healthcare. In this role he strove to ensure a patient-centered culture while focusing on healthcare providers and his team was embedded in all facets of the business; R&D, clinical trials, training, compliance, business development and risk management.

He continues a clinical practice at Massachusetts General Hospital and an academic affiliation at Harvard Medical School, both in Boston. He continues to publish and has recently been granted several more patents. He is co-leader of an annual mission to Vietnam where he provides care to children and medical teaching to those who care for children.

Steve Schwaitzberg, MD, FACS, is an advisor to Arch, bringing his expertise in surgery, clinical trials, and biomaterials for hemostasis and sealing. He is Professor of and Chairman the Department of Surgery for the University at Buffalo - Jacobs School of Medicine and Biomedical Sciences. Formerly he was the Chief of Surgery at Cambridge Health Alliance, adjunct professor at Tufts University, and Professor of surgery at Harvard Medical School. He is Past President of the Society of American Gastrointestinal Endoscopic Surgeons (SAGES), a world-class laparoscopic surgical association.

A key opinion leader, Dr. Schwaitzberg has a distinguished reputation in surgery. He was initially trained as a trauma and surgical infection expert and then became an early leader in the minimally invasive surgery (MIS) revolution. Dr. Schwaitzberg is an innovator who teaches surgical technique around the world. He has served in key leaderships positions in major surgical organizations and received international recognition as a leader in technology in the operating room and for the introduction of novel MIS technology.

Dr. Schwaitzberg is a seasoned clinical researcher who also served as the Chairman of the Tufts University School of Medicine and Medical Center institutional review Board. He has a deep interest in technology development. He is widely published and has been invited to present and teach courses around the world for over 25 years. Dr. Schwaitzberg earned an MD from Baylor College of Medicine, a MA from Harvard medical School and a BA in biology from The Johns Hopkins University.

Dr. Paresh Shah is the Director of General Surgery and Vice Chair of Surgery at the NYU Langone Medical Center, and Professor of Surgery at the NYU Langone School of Medicine. Dr. Shah has a special interest in diseases of the pancreas, stomach and colon and his clinical practice is focused on advanced laparoscopic surgery including bariatrics, hernia, and GI surgery. As an internationally renowned leader in minimally invasive surgery, Dr. Shah was one of the pioneers in applying laparoscopic approaches to GI cancer resections, including totally laparoscopic pancreatectomy and gastrectomy.

Dr. Shah's expertise extends to healthcare management and quality. He served as CMIO at the Lahey Clinic, Director of Quality in the Departments of Surgery at Lenox Hill Hospital and NYU Langone Medical Center; He is the Chair of the Surgical Committee of the Value Based Management Task Force at NYU. Dr. Shah has also brought his leadership skills to professional societies, including the American College of Surgeons, the Society of Surgery of the Alimentary Tract (SSAT), and the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) where he is on the Board of Governors. He has worked with national policy groups, including the Presidential Task Force for Health Care IT, and was a Specialty Advisor to the Current Procedural Terminology (CPTÒ) Editorial Panel of the American Medical Association (AMA).

Dr. Shah is also a thought leader in technology development, entrepreneurship, and commercialization in the healthcare arena. He was a founder of 3 medical device and healthcare startups, and has consulted for early stage companies as well as some of the largest companies in the healthcare sector including Stryker, Olympus, Medtronic and Ethicon.

Elaine Whitmore, PhD, brings over 25 years of extensive history in the medical products industry to Arch Therapeutics, with whom she started working in late 2010 focusing on regulatory planning and strategy. In addition to regulatory submissions, Dr. Whitmore’s experience includes development, testing, technology evaluation, and clinical planning for a variety of hemostasis products (fibrin sealants; bovine, human and recombinant thrombin products; cellulose; collagen; etc.), adhesion prevention products, and infection prevention products.

Dr. Whitmore is the author of Development of FDA-Regulated Medical Products—A Translational Approach (ASQ Quality Press, 2012) and has numerous patents for medical product technologies. Prior to becoming a product development and technology consultant, she held executive management industry positions in a variety of functions, including New Product Development, Regulatory and Clinical Affairs, Scientific Affairs, and Business Development. Dr. Whitmore received her PhD degree from Northwestern University.