Ben Bahavar, Ph.D.
Ben Bahavar, Ph.D.
Ben Bahavar, Ph.D., is an experimentalist researcher with multidisciplinary training and 17 years of experience in applied chemistry, semiconductor materials, and chemical engineering. His analyses help companies assess new applications of products and processes, seek solutions to technical problems, and perform feasibility studies. Read more.
Robert M. Beinstein, P.E., ENV SP
Robert M. Beinstein, P.E., ENV SP
Robert M. Beinstein(Bob) is a mid-career engineering graduate of UCONN, who has taken on technical and managerial roles in the commercial nuclear industry, managed environmental and smart growth programs in the Federal marketplace, and lead a diverse array of business development and client service-related work in the engineering consulting business. Read more.
Erica Kramer, Ph.D.
Erica Kramer, Ph.D.
Dr. Erica Kramer works primarily with the Medical Device team at Nerac conducting research of clinical literature, preparing clinical literature evaluations, and conducting focused research to address clients’ questions relating to the medical device industry. Read more.
Jeffrey Magee, BSME, MBA
Jeffrey Magee, BSME, MBA
Jeffrey Magee, BSME & MBA, helps clients identify, secure and expand their intellectual property assets while defining market niches using engineering and business metrics. Read more.
Helga Weires
Helga Weires
Analyst Helga Weires works with medical device manufacturers, academics, and individual physicians from around the world developing diagnostic and therapeutic devices. She guides clients through technical and intellectual property issues regarding medical devices for all branches of medicine, including orthopedics, cardiology and internal medicine. Read more.
Mary Becher
Mary Becher
Analyst Mary Becher specializes in metallurgical process testing and quality control, assisting companies in the specialty materials industry. Read more.
Minh Han, MD, FAAFP
Minh Han, MD, FAAFP
Dr. Minh Han is part of the medical device regulatory team at Nerac evaluating clinical literature, drafting clinical evaluation plans (CEPs), and preparing clinical evaluation reports (CERs), with a particular focus on State of the Art. Read more.
Priscilla S. Monarca
Priscilla S. Monarca
Priscilla S. Monarca is a member of the medical device regulatory team at Nerac and works with medical device companies to conduct client-specific research, including literature reviews, and prepare reports and other support services to meet client needs. Read more.
Richard Hendriks, Ph.D.
Richard Hendriks, Ph.D.
Analyst Richard Hendriks, Ph.D., partners with pharmaceutical and biotech companies to discover the most effective ways of meeting their business goals. This encompasses a range of solutions from innovations in biotechnology to analytical assessments of recent treatment advances. Read more.
Richard Maldanis, Ph.D.
Richard Maldanis, Ph.D.
For over a decade, Richard Maldanis, Ph.D. has been assisting Nerac clients in the specialty chemistry and material science fields. His diverse expertise in organic, inorganic, organometallic and polymer chemistry provides clients with solutions to a broad range of chemistry-related challenges. Read more.
Rosemarie Szostak, Ph.D.
Rosemarie Szostak, Ph.D.
Analyst Rosemarie Szostak, Ph.D., advises companies on technology, patents, innovation and disruptive technology. She has 20 plus years as a thought leader and analyst with broad technical knowledge in chemistry, materials and chemical engineering. Read more.
Ryan Rix
Ryan Rix
Analyst Ryan Rix brings experience in Human Biology, General Chemistry, Pharmaceutical Compliance and Regulatory Affairs. Read more.