Rule He-P 307: Creating an Immunization Central Registry

New Hampshire
New Hampshire

Last Updated: April 30, 2014
Rule He-P 307: Creating an Immunization Central Registry
Department of Health and Human Services

He-P 307 create a new database that would track New Hampshire residents' personal medical information. The proposed rule would require medical providers to submit the names, immunization status and over 75 other data points of children and other persons immunized in the state of New Hampshire.

Under the proposed rules, the registry will collect and store the data and provide access to the information to any person or agency authorized by the state who is concerned with the immunization or health-care screening of children. While the registry is required to keep these immunization records confidential, one of the central purposes for creating the statewide immunization registry is to provide the immunization status of children available to all authorized users, including local health districts, health-care providers, schools, and local social services district responsible for the care and custody of the children.

HSLDA's Position:

HSLDA is concerned that this database could result in significant privacy violations. Parents, not the government should be managing children's medical information and not through a state-wide database. Even if such a program were viable, at the very least it should be voluntary and operate as an “opt-in” program where people have to affirmatively give their permission for information to be stored, rather than an “opt-out” where a person must navigate a cumbersome opt out process in contact with the Department of Health and Human Services.

Action Requested:
None at this time

Open to public comments until May 29, 2014.

Public Hearing on Thursday, May 22 at 1:30 p.m.
Auditorium of the DHHS Brown Building
129 Pleasant St.
Concord, NH 03301


Many parents are concerned about the medical risks of vaccinations. Parents, not the government, should have the right to make medical decisions, such as vaccinating their children. Parents should also have the ability to choose whether or not to place their children's immunization history on an immunization registry. Making it harder to opt out of placing sensitive medical information on a registry restricts a parent's right to monitor their children's medical history. If this rule passes, many parents may become unaware that they can opt of sharing their children's immunization history.

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