Given the recent Health Canada’s rules on medical device classification rules and the requirement for all patient management to be certified as class II has an impact on vendors/distributors selling products in Canada.
This is quite an important event for both the customers and vendors to understand the new requirements and network with others who are undergoing the process.
This event is organized by Ontario HIMSS chapter and the first time the chapter is organizing an event of this size, which is quite an amazing feet. Kudos to the organizers and I wish them all the success.
Plus: Low registration fee and you can network with regional health leaders to understand where eHealth is marching towards in Canada.
EMR / HIS market entry through acquisition from a foreign player looked never feasible given how healthcare delivery is unique to each country with the regulations, structure ( public versus private), clinical workflows and business processes associated with it. Even between US and Canada there is quite a difference though Meditech has significant presence in both countries due to various reasons.
Healthcare IT is quite brimming with lots of activities with the healthcare stimulus package in the US through ARRA and HITECT act and deadline looming (effective from October 2010) for healthcare providers(hospitals, group practitioners, imaging centers) and eligible professionals (physicians) to get their slice of the pie.
Healthcare IT vendors welcome the final rule – of course – industry is going to get even busier with the set targets for the years 2010 and 2010
My brief and quick analysis:
1. Coordinated release of Meaningful Use and Standards requirements final rule
While the meaningful use represents the functional requirements ( the WHAT piece) that has to be met by the providers, the coordinated release of HHS final rule on standards, implementation specification and certification criteria ( the HOW piece) is a commendable job by the people at CMS and HHS.
For example there are requirements in final meaningful use on submitting immunization and laboratory data to public health agencies and providing patients with timely access to their electronic health data
HHS final rule on standards requires using existing penetrated (both from providers, vendors and available resources in the market perspective) standards like HL7 version 2.3.1, 2.5, HL7 CDA to accomplish exchange of information between providers and public health agencies and transferring data to patients.
This enables the providers, vendors to use existing standards to reach compliance on various functional requirements in meaningful use from a technical perspective.
I will follow up with frequent updates as I consume the bulk documents on meaningful use and HHS standards requirements and the nuances of implementation requirements.
Exciting times ahead in the Healthcare IT industry indeed and also I am starting to lead a delivery work on an eReferral project in the province of Ontario to enable physicians to refer patients to their specialist electronically rather than current way of phone calls, faxes and hodgepodge of activities.
The announcement reads “With newly opened government data sets and lightweight frameworks for rapid application development, we have a unique opportunity to participate in an ecosystem of data “suppliers” and “appliers” to build innovative tools to improve personal and population health”.
This sounds very similar to the CIHI (Canadian Institute for Health Information) in Canada, which is a govt. funded organization that analyzes data from the ecosystem of healthcare providers and community organizations to report and improve personal and population health.