Martin Sklar President & CEO AblaCor™ Medical Corporation

AblaCor is led by Martin Sklar, founder & CEO, a highly accomplished Leader, Inventor, Consultant
and Engineer. He has extensive experience in business development, intellectual property
development, project management, design engineering, manufacturing engineering, technical
analysis, and product introduction in the medical technology industry. He founded Automated
Medical Instruments, Inc. in 1992, now AblaCor Medical Corporation as of January 2013, to focus on
developing remote controlled instruments for minimally invasive medical applications, including the
current activities to treat Atrial Fibrillation.

Adrian Orr

Adrian Orr is the Executive Director of Clinical Affairs at Anika Therapeutics, Inc in Bedford, MA. Adrian has previously worked in a range of small to medium-sized medical device and biologics companies including Gyrus Medical, Serica Technologies, and Haemonetics. He has focused on re-structuring and developing clinical teams to tackle technically challenging surgical and biologics trials. Adrian’s current focus is on joint preservation and tissue regeneration in orthopedics. His talk today will center on the use of eDiaries in clinical research.

Jerrold Shapiro

My work with gynecologists, nurse practitioners, physical therapists, other healthcare providers and their patients since 2002 in the treatment of female urinary stress and mixed incontinence made me keenly aware of how urinary incontinence reduces the quality of patients’ lives.  Despite the high efficacy of the pelvic floor exercise device we rented to them, patients with mild dementia could not remember the protocol, those with MS and paraplegia could not contract their pelvic floor muscles (PFM) and younger women busy with work and family responsibilities did not have the time to exercise.  Cheri Grantham, an experienced medical assistant, and I began developing a medical device which blocks unwanted urine leaks and does not require exercise or the cooperation of the patient.  I bring to this task over fifty one years of medical device experience, both in academia, private industry and consulting.  I have the leadership and technical skills, industry contacts and FDA experience to take this device all the way into the market so that we can greatly improve the quality of life of not just incontinent women, but of their caregivers and families, as well as saving third party payers such as Medicare a significant sum now paid to institutionalize some of these patients due to their incontinence, as well as funds paid for surgery and absorbent products. In previous positions I designed and ran local and international clinical trials of medical devices that diagnosed or treated eye diseases and skin conditions. Our team is currently navigating the difficulties COVID-19 has created for running a clinical study, both indirectly by keeping subjects home and directly by infecting one of our team members.

Simon Jones

Simon has 20 years of experience in delivering product strategies and product positioning which address market opportunities effectively. He is a subject expert in clinical trials labeling, researching this market, discussing the industry challenges with the PRISYM ID customers and remaining up to date on market trends, regulatory changes and technology alternatives.

Carl Olén

CEO & board member at Skogsfond Baltikum

9 years experience from Baltic forest investments.

Fund Manager at AIFP Baltic Asset Management for Skogsfond Baltikum, chairman of Latvijas Mezu Agentura  which is subsidiary to Skogsfond Baltikum. Chairman of SIA Lettskogolen that controls 1070 hectars of forestland in Latvia. Board member of acquisition and forest management company SIA Kupica. Owner and investment advisor in Forest Value AB. Board member of wind energy company Rockagården Vind AB.

Background: B.Sc. Business Administration, Uppsala University. Previously Head of Controlling & Business Development at Scania CV AB.

Jay Russak

Jay has over 17 years of clinical development experience.  He currently is the clinical lead for the PAH program at Keros Therapeutics.  He has been working at smaller biotech companies for the last 8 plus years.  In addition, he is an adjunct faculty member at Northeastern University teaching in the Masters of Regulatory Affairs program.