Webinars

Mr. Leslie Bihari, Jr. is a seasoned clinical trial professional with a Bachelor’s Degree in Biological Sciences from Cornell University and a Bachelor’s in Mechanical Engineering from the SUNY at Buffalo NY. Mr. Bihari has been providing software and biotechnology solutions to industry for over 20 years. Upon entering the clinical trials space Mr. Bihari found an opportunity to blend two passions – software and science. After managing both services and sales for Phase Forward a leading provider of software for the clinical trial industry, Mr. Bihari founded his own company, eClipse Enterprise Solutions. He has grown the company from a small consulting boutique to a full service CRO, providing clinical trial management services worldwide.

Mrs. Kristie Lively has over 20 years of experience in the life sciences industry. Her career has been dedicated to clinical operations and quality compliance, including all phases of CRO service operations and management . Her leadership and commitment to quality allows for a deep understanding of customer needs and quality service delivery. She previously served as CRO Vice President for two clinical research organizations, conducting community-based clinical trials in oncology and oncology early drug development. Mrs. Lively received her Bachelor of Science in Nursing degree from the University of Memphis.

Mr. Linstad’s Clinical Technology career includes executive roles in the development and execution of global Clinical and Healthcare initiatives. With a Bachelor’s of Science Degree in Electrical and Computer Engineering from Merrimack College, Mr. Linstad leads, develops and directs the strategic clinical and healthcare technology operations for the clients of Eclipse Clinical Technology. Prior to joining Eclipse Clinical Technology, Mr. Linstad was employed by Phase Forward where he designed clinical solutions built on Phase Forward software (now Oracle Healthcare) to integrate with customers’ existing technical and non-technical processes.

Dr. Deiter Schlaps has over 25 years of regulatory experience and is currently a contributing member within the Workgroup 6 (“Pharmacy and Medicines Business”) of ISO’s Technical Committee 215 (“Health Informatics”) as a Delegate of DIN “Deutsches Institut fuer Normung”. Dr. Schlaps specializes in Regulatory Information and Document Management and has held management positions at IABG Ottobrunn, CSC Germany GmbH, Logica Germany and NNIT Germany GmbH. He has worked on customer projects at: Heel, Astellas, Bayer AG, Merck KGaA, MSD, Boehringer Ingelheim, Takeda, Roche, Novartis, BASF AG, Abbott, Röhm Pharma, Almirall, Pfizer, Grünenthal, Novo Nordisk etc.  Dr.Schlaps most recent projects include support for an IDMP Gap Analysis, Roadmap for a Sharepoint-based solution for the sharing of Batch Manufacturing Quality Documentation and IDMP Pre-Project and IDMP Training.