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The Health Information Security and Privacy Collaboration (HISPC)

Established in June 2006 by RTI International through a contract with the U.S. Department of Health and Human Services (HHS), the Health Information Security and Privacy Collaboration (HISPC) originally comprised 34 states and territories. HISPC phase 3 began in April 2008, and HISPC now comprises 42 states and territories, and aims to address the privacy and security challenges presented by electronic health information exchange through multi-state collaboration. Each HISPC participant continues to have the support of its state or territorial governor and maintains a steering committee and contact with a range of local stakeholders to ensure that developed solutions accurately reflect local preferences.

The third phase, comprises 7 multi-state collaborative privacy and security projects focused on analyzing consent data elements in state law; studying intrastate and interstate consent policies; developing tools to help harmonize state privacy laws; developing tools and strategies to educate and engage consumers; developing a toolkit to educate providers; recommending basic security policy requirements; and developing inter-organizational agreements.

Each project is designed to develop common, replicable multi-state solutions that have the potential to reduce variation in and harmonize privacy and security practices, policies, and laws.

Click on the boxes below to view more details about the Collaboratives and their products.

Consumer Education and Engagement   Provider Education

Harmonizing State Privacy Law   Intrastate and Interstate Consent Policy Options   InterState Disclosure and Patient Consent Requirements

Inter-Organizational Agreements   Adoption of Standard Policies

HISPC Reports on State Law, Business Practices, and Policy Variations

Conducted during 2009 as part of the Health Information Security and Privacy Collaboration (HISPC), the following compendium of 5 reports detail variations in state law, business practices and policy related to privacy and security and the electronic exchange of health information.   For quick reference, several reports contain aggregate findings tables in their appendices.  Summaries of each report are below.

**For citation purposes, please use the date the reports were published and released to the public: January 13th, 2010.**

This report analyzes state laws that are intended to require health care providers (specifically, medical doctors and hospitals) to afford individuals access to their own health information and to identify potential barriers to the electronic exchange of health information.  Specific state law provisions examined: scope of medical records to which patients are afforded access, format of information furnished, deadlines for responding to requests, fees for furnishing copies, record retention laws and access to records of minors.

This report identifies and analyzes the impact and variation of state laws related to e-prescribing.  The report addresses state laws related to the e-prescribing of controlled and non-controlled substances as well as topics such as record keeping and content requirements, out-of-state prescriptions, and generic substitution laws.

  • Perspectives on Patient Matching: Approaches, Findings, and Challenges [PDF - 629 KB]
    This report analyzes various approaches to matching patients to their health information in the context of electronic health information exchange.  Current and potential methods for matching patients to their health records are discussed, challenges to performing patient matching such as scalability and ease of use are analyzed, and the types of information some HIOs use to match patients to their health records is described.
2010/04/09
Action and Implementation Manual

Action and Implementation Manual (AIM)

The AIM serves as a how-to guide for each of the seven multistate collaboratives' tools and templates.