OTech has access to several industry experts and consultants who are used to create a team to solve your training and consulting need. Our core OTech associates include the following professionals.
He functions as the EHR, PACS, DICOM, and IHE instructor as well as a consultant and overall project manager for most of the projects. He is very familiar with the PACS industry and technology because of his prior work experience as a PACS program and business unit manager with Philips, AT&T, and Kodak. His EMR experience is mainly through his involvement with the IHE community and being actively involved with EMR selection and implementation through his work at local community clinics. He teaches and publishes extensively on PACS and related topics such as the DICOM standard. He participates with the DICOM, HL7 and IHE standardization efforts serving in various positions and working groups. View Resume
Johanna has a background in the healthcare field ranges from being a RN, working in anesthesiology, to practicing as a licensed hypnotherapist and teach about alternative medicine and energy work. For OTech, she handles accounts payable and receivables. She is also responsible for all seminar coordination, including registration and she maintains our corporate database. If you have any questions about our products our services, do not hesitate to contact her via phone or e-mail and she will be able to help you and/or refer you to the right person.
Carl T. Alletto, M.S.
Senior Regulatory Consultant
Carl is a Certified Professional Consultant, ASQC Certified Quality Manager, Certified Software Quality Engineer, and Certified Quality Auditor. Carl is our consultant who prepares all of our regulatory (FDA) filings, interacts with the FDA, performs our audits, and provides support and assistance on regulatory affairs. He offers a broad range of experience and expertise in the development, implementation, and assessment of medical device regulations, software quality, verification/validation, ISO 9000 certification, and FDA Good Manufacturing Practices. With over 20 years experience in a Fortune 500 company as Director of Regulatory Affairs and Vice President of Quality, he understands PACS medical device regulations 510(k) guidelines, compliance, and quality standards that are critical to a your business. View Resume
Tim is responsible for developing the back-end of our website.
Suzanne is responsible for our order processing, shipping and handling, our customer support and all of our seminar materials such as binders and multimedia creation. She has an extensive background in various support positions for several organizations.
HL7 V2 Instructor
Ted Klein has been involved with the HL7 standardization effort since its inception. He has been active in various leadership roles and participated in many of the working groups creating parts of the standard. He has worked as chief technical scientist and senior technical fellow in the industry for many years and works and an independent consultant to assist many organizations defining, specifying and implementing healthcare IT technologies. He is the HL& representative to the ISO TC215, member of the clinical LOINC committee, and past HL7 vocabulary chair.
Brett Marquard is an interoperability analyst specializing in the design and development of healthcare data exchanges. He is a co-chair of Health Level Seven's (HL7) Structured Document Working Group (SDWG) and Primary Editor of the HL7 Consolidated Templates Draft Standard. The Office of the National Coordinator (ONC) recently named the Consolidated Templates DSTU in Meaningful Use Stage 2. Brett is a liaison from the SDWG to the HL7 Claims Attachments Work Group. Brett trains new implementers, developers, and policy makers on the Clinical Document Architecture (CDA), and HL7 version 2.
Chris is responsible for developing the front-end of our website.
Lisa Nelson is an independent medical informatics consultant with over 20 years of experience. She is an HL7 Certified CDA Specialist, and has extensive experience validating CDA R2 implementation specifications for the IHE's Quality, Research, Public Health domain and Patient Care Coordination domain. She participated in the CDA Consolidation project for the S&I Framework initiative. As an active member of HL7 and IHE, she contributes to the development of national standards for the use and exchange of digital health records and clinical quality measures.
John Sole, CIIP & CPAS
John has both a clinical and IT background and has worked in the PACS industry both at the user and vendor side for ten years. His careers include CT technologist, PACS system specialist, PACS administrator, systems engineer and technical solutions architect.
You can contact any of our associates through email@example.com.
Advanced PACS, DICOM, HL7 Troubleshooting
Fundamentals of Clinical and IT (PARCA CPAS)
PACS System Administration
Comprehensive HL7 (V2)
CDA IN A DAY (HL7 V3)
Certified EMR Administrator Training
Click here to view entire training schedule.
Click here to view the latest video regarding the DICOM sniffer.