Dr. Kosta Makrodimitris, PhD, CF-FDA, CP-EHR, is Biomedical/Health Informatics Advisor, Author & Strategist. He is certified on EHR/PHR, Clinical Trials, Biotech/Drug Development, and trained in US FDA/DHHS laws, regulations (medical devices, foods, drugs, personalized medicine, health IT). He is involved as:
- Advisor and participant (ONC/DHHS for Health IT, Standards & Interoperability Framework, Meaningful Use Stages/EHR, Federal Health Architecture, Health Information Exchanges-HIMSS, Health Level 7/ISO TC215 standards).
- Executive director of Global Bio Health Tech Center and senior policy advisor at CAL2CAL group of companies
- Medical Devices Committee Member, Author at The Food and Drug Law Institute,
Dr. Makrodimitris combines a multidisciplinary background and accomplishments in Health IT/Informatics, Policy, Standards and Innovation http://www.linkedin.com/in/kostamakrodimitris
- In academia (Johns Hopkins, University of Virginia, EU), I researched concerning biomedical applications and bio-chem- informatics.
- In industry (FannieMae, Sysco/Sentrana, MakronanoKosmos, Cal2Cal) I designed innovative decision systems, managed analytics projects, cofounded eHealth business, consulted business development, provided policy analysis.
- In government (US-FDA/DHHS), I trained and worked in regulatory science, enterprise architecture, standards, and policy in public health and health IT. I served as Program Manager, for Maryland BioTechnology Center, Business and Economic Development.
