PHIA - Questions and Answers
PHIA - Questions and Answers
February 2005
Dr. Ann Cavoukian, the Information and Privacy Commissioner of Ontario, gratefully acknowledges the work of Sylvia Klasovec and Mark Ratner in preparing this document. This FAQ provides a general overview of the Personal Health Information Protection Act, 2004, S.O. 2004, c.3. and Regulation 329/04. The information contained in this document is for general reference purposes only and should not be construed as legal advice. You should consult with your own solicitor for all purposes of interpretation. This publication is also available on the IPC website. Cette publication est galement disponible en franais.
Table of Contents
Background .......................................................................................................... 1 Introduction ......................................................................................................... 2
What is the Personal Health Information Protection Act, 2004 (PHIPA)? .................... 2 When did PHIPA come into force? ............................................................................. 2 Is PHIPA retroactive? .................................................................................................. 3
Overview .............................................................................................................. 4
What is the purpose of PHIPA? .................................................................................. 4 Why do we need a health privacy law in Ontario? ..................................................... 4 What is the relationship between PHIPA and the federal Personal Information Protection and Electronic Documents Act (PIPEDA)? ............ 5
What is the responsibility of a health information custodian who works for a non-health information custodian? ............................................ 14
Research ............................................................................................................. 27
What are the requirements for the collection, use and disclosure of personal health information for health care research? ...................................... 27 Are there any requirements for research ethics boards and research plans?............... 28
Can a health information custodian refuse to correct an individuals personal health information? ........................................................ 34
Background
The Health Information Protection Act, 2004 was introduced in the Legislature on December 17, 2003 and received Royal Assent on May 20, 2004. The legislation contains two schedules: the Personal Health Information Protection Act, 2004 (Schedule A) and the Quality of Care Information Protection Act, 2004 (Schedule B). Together, these schedules comprise the Health Information Protection Act, 2004. This FAQ will address the Personal Health Information Protection Act, 2004 (PHIPA).
Introduction
What is the Personal Health Information Protection Act, 2004 (PHIPA)?
The Personal Health Information Protection Act, 2004 (PHIPA) is Ontarios new healthspecific privacy legislation. PHIPA governs the manner in which personal health information may be collected, used and disclosed within the health care system. It also regulates individuals and organizations that receive personal information from health care professionals. PHIPA creates a consistent approach to protecting personal health information across the health care system. By providing a level playing field for all health care professions, PHIPA builds upon and codifies many of the existing high standards and protections enshrined in the common law, various professional codes, policies and guidelines. These legislated rules were designed to give individuals greater control over how their personal health information is collected, used or disclosed. They provide health care professionals with a flexible framework to access and use health information as necessary in order to deliver adequate and timely health care. In addition, PHIPA confirms a patients existing right to access ones own personal health information and provides a means for redress through the Office of the Information and Privacy Commissioner/Ontario (IPC) when privacy rights relating to personal health information have been violated. The IPC has been designated as the oversight body responsible for administering and enforcing these new health sector privacy rules. As such, we have prepared the following questions and answers to guide Ontarians and health care professionals in understanding their respective privacy rights and obligations.
Is PHIPA retroactive?
No. PHIPA applies to the collection, use and disclosure of personal health information by health information custodians as of November 1, 2004. There is no obligation for custodians to seek consent for personal health information that was collected prior to this date. However, a health information custodian must obtain consent for the use or disclosure of that information after November 1. In addition, as of November 1, 2004, PHIPA will apply to the use and disclosure of personal health information by any person who is not a health information custodian and who has received the information from a custodian, before or after this date.
Overview
What is the purpose of PHIPA?
PHIPA establishes a set of uniform rules about the manner in which personal health information may be collected, used or disclosed, and includes provisions that: Require consent for the collection, use and disclosure of personal health information, with necessary but limited exceptions; Require that health information custodians treat all personal health information as confidential and keep it secure; Strengthen an individuals right to access his/her personal health information, as well as the right to correct errors; Give a patient the right to instruct health information custodians not to share any part of his/her personal health information with other health care providers; Establish clear rules for the use of personal health information for fundraising or marketing purposes; Set guidelines for the use and disclosure of personal health information for research purposes; Ensure accountability by granting an individual the right to complain to the IPC about the practices of a health information custodian; and Establish remedies for breaches of the legislation.
of a medical emergency. Beyond patient care, personal health information is needed for important activities such as health research vital to develop new treatments and cures. The increasing use of technology to transfer and store medical data instantaneously has also increased the need for legislated rules to assure Ontarians that their personal health information will be strongly protected.
What is the relationship between PHIPA and the federal Personal Information Protection and Electronic Documents Act (PIPEDA)?
The collection, use and disclosure of personal information within the commercial sector is regulated by federal privacy legislation the Personal Information Protection and Electronic Documents Act (PIPEDA). PIPEDA was enacted to regulate the collection, use or disclosure of personal information in the hands of private sector organizations. As of January 1, 2004, PIPEDA has applied to all Ontario private sector organizations, including pharmacies, laboratories, and health care providers with operating practices that qualify as commercial activities. PIPEDA does not apply to personal information in provinces and territories that have substantially similar privacy legislation in place. The application of PIPEDA to personal health information has raised a number of concerns. The requirements under PIPEDA were designed to regulate direct marketing, electronic commerce and other analogous activities and do not specifically address the unique circumstances encountered within the health care system. The federal government is expected to deem the provisions of Ontarios PHIPA to be substantially similar to PIPEDA in order to exempt health care providers that are covered under PHIPA from also having to comply with the provisions of PIPEDA. However, even if such an exemption is made, PIPEDA will continue to apply to all commercial activities relating to the exchange of personal health information between provinces and territories and to information transfers outside of Canada.
Laboratories; Nursing homes and long-term care facilities; Homes for the aged and homes for special care; Community care access corporations; Ambulance services; Boards of health; The Minister of Health and Long-Term Care; and The Canadian Blood Services. A health information custodian does not include: An aboriginal healer or aboriginal midwife who provides traditional healing services to aboriginal persons or members of an aboriginal community; and A person who provides treatment by spiritual means or by prayer.
What is an agent?
PHIPA defines an agent to include any person who is authorized by a health information custodian to perform services or activities on the custodians behalf and for the purposes of that custodian. An agent may include an individual or company that contracts with, is employed by or volunteers for a health information custodian and, as a result, may have access to personal health information. PHIPA permits custodians to provide personal health information to their agents only if the custodian is permitted to collect, use, disclose, retain or dispose of the information. For example, an agency relationship under PHIPA includes a nurse who is employed by, or a medical student who volunteers at, a hospital. An agency relationship may also include a physician who is not employed by a hospital but has admitting privileges to use the hospitals equipment or facilities. In such cases, the custodian hospital is permitted to authorize the agent to handle or deal with personal health information on its behalf so long as the agent complies with PHIPA and adopts the information practices of the custodian.
Blood or body-part donations; Payment or eligibility for health care; and The identity of a health care provider or a substitute decision-maker for the individual. Identifying information includes health information that could identify an individual when used alone or in conjunction with other information. Personal health information does not include identifying information about an employee or agent of the custodian that is not maintained for the provision of health care. For example, a doctors note to support an absence from work in the personnel file of a secretary employed by a health information custodian is not considered personal health information.
are permitted to disclose personal health information without consent to these listed persons. They consist of the following: Cardiac Care Network of Ontario in respect of its registry of cardiac services; INSCYTE (Information System for Cytology) in respect of its registry of CytoBase; London Health Sciences Centre in respect of the Ontario Joint Replacement Registry; and Canadian Stroke Network in respect of the Registry of the Canadian Stroke Network. The above-noted registries may use and disclose personal health information for the purpose of facilitating or improving the provision of health care or for the storage or donation of bodily substances. They are also permitted to use and disclose personal health information for research purposes with a research plan approved by a research ethics board (REB) in certain circumstances. These persons are also permitted to disclose personal health information to prescribed entities for the planning, management or analysis of the health system. The regulations also require that registries make publicly available: A plain language description of the functions of the registry; and Practices and procedures approved by the Commissioner to protect the security and confidentiality of the personal health information that it receives. What is a prescribed entity? The regulations prescribe a list of entities, including any registries maintained within these listed entities, that health information custodians are permitted to disclose personal health information to without consent for the purposes of planning and management of the health system. Prescribed entities consist of the following: Cancer Care Ontario (CCO); Canadian Institute for Health Information (CIHI); Institute for Clinical Evaluative Sciences (ICES); and Pediatric Oncology Group of Ontario (POGO).
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In certain circumstances, with a research plan approved by a research ethics board, these prescribed entities are permitted to use and disclose personal health information for research purposes as if they were health information custodians. A prescribed entity is also permitted to disclose personal health information to a prescribed person who compiles or maintains a registry of personal health information, and for purposes related to the planning, management and analysis of the health care system. These entities must make publicly available a plain language description of the functions of the entity, including a summary of the practices and procedures approved by the Commissioner for maintaining the confidentiality of the information.
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Provide a written statement that is readily available to the public and describes: A custodians information practices; How to reach the contact person; and How an individual may obtain access, request a correction or make a complaint regarding his/her personal health information. Inform an individual of any uses and disclosures of personal health information without the individuals consent that occurred outside the custodians information practices; and Ensure that all agents of the custodian are appropriately informed of their duties under PHIPA.
What is the responsibility of a health information custodian who works for a non-health information custodian?
A health care practitioner who has custody or control over personal health information but who contracts with, is employed by or volunteers for an organization that is not defined as a health information custodian under PHIPA, is not an agent. In such a circumstance, the individual would fall within the definition of a health information custodian under PHIPA and must ensure compliance. Examples of health information custodians who work for non-health information custodians include: A nurse employed by a school board to provide health care services to students; A doctor employed by a professional sports team in order to diagnose sporting injuries; A registered massage therapist providing health care services to clients of a spa; and A nurse employed in-house by a manufacturing firm in a health care capacity.
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Consent Requirements
What is consent under PHIPA?
The general rule is that a health information custodian needs to obtain an individuals consent to collect, use and disclose personal health information unless PHIPA allows the collection, use or disclosure without consent. An individuals consent may be express or implied.
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Are pharmacists required to obtain express consent from an individual to disclose personal health information to a third party benefits payor?
No. The regulation provides an exception to the express consent requirement where a pharmacist discloses personal health information to a third party who is not a health information custodian and who is being asked to provide payment for a medication or related goods or services provided to an individual. Pharmacists are permitted to rely on an individuals implied consent if they provide or post a notice that explains how an individuals personal health information is used and to whom it will be disclosed.
Can an individual control what personal health information is recorded in his/her file?
Yes, but any condition placed on the collection, use or disclosure of personal health information cannot prohibit the recording of personal health information that is required by law, professional or institutional practice.
What is a lock-box?
The lock-box is not a defined term under PHIPA. It is a term of reference used to describe the right of an individual to instruct a health information custodian not to disclose specified personal health information to another custodian for the purpose of providing health care. An individual can be said to have placed his/her personal health information into a lock-box by expressly withholding or withdrawing consent for his/her health information to be collected, used or disclosed.
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PHIPA lists, in order of priority, the following substitute decision-makers who may consent on behalf of an individual when consent is required, including: The guardian of the person or of the property; The attorney for personal care or property; The representative appointed by the Consent and Capacity Board; The spouse or partner; A child or parent (including the Childrens Aid Society); A parent who has right of access; A sibling; A relative; and as a last resort The Public Guardian and Trustee.
Can another person, such as a family member, provide consent on an individuals behalf when picking up or dropping off a prescription?
Yes. The regulations permit a pharmacist to provide a prescription to another person unless the prescriber (a physician, for example) states otherwise. This is also permitted under the Drug and Pharmacies Regulation Act.
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What are the rules regarding the collection of personal health information? Health information custodians within the circle of care may rely on an individuals implied consent to collect personal health information for the purpose of providing health care. With limited exceptions, health information custodians must collect personal health information directly from the individual involved and may only collect as much information as is necessary to meet the purpose of the collection. Custodians must take reasonable steps to inform the public about their information practices and how individuals may exercise their rights under PHIPA. Some suggested methods of meeting this requirement include the use of visible brochures, posters, notices posted on walls and verbal explanations.
What are the exceptions to the rules for collecting personal health information? PHIPA provides for the collection of personal health information directly from individuals. Health information custodians may collect personal health information indirectly where, for example: The individual consents; The collection is necessary for providing health care and it is not possible to obtain the information directly from the individual in a timely manner; The custodian collects personal health information for the purposes of research from a person who is not a health information custodian, provided that certain conditions are met;
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The indirect collection is required or permitted by law; The indirect collection is required for the purpose of health planning or management; or The IPC authorizes the indirect collection.
Use
What is a use of personal health information under PHIPA? Use of personal health information under PHIPA is defined as the handling or dealing with personal health information that is in the custody or control of a health information custodian or its authorized agent. This includes accessing or reproducing health information as required by the custodian.
What are the rules regarding the use of personal health information? As a general rule, consent is required for any use of an individuals personal health information unless PHIPA allows the use without consent. A health information custodian may rely on an individuals implied consent to share personal health information with its authorized agent, as long as the sharing is related to the provision of health care and the individual has not expressly stated otherwise. When using personal health information, a custodian must exercise the highest level of care and must take reasonable steps to ensure that the individuals personal health information is as accurate, complete and up-to-date for the purpose which the custodian uses the information. Where a health information custodian is authorized to use the information, the custodian may provide the information to an agent of the custodian to use it for that purpose on behalf of the custodian. The sharing of information between a custodian and its agent is considered to be a use and not a disclosure for the purposes of PHIPA.
What are the exceptions to the rules regarding the use of personal health information? PHIPA sets out a limited set of acceptable uses of personal health information without consent, including for the following purposes:
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Risk management, error management, or activities to improve or maintain the quality of care or any related program or service; Educating agents to provide health care; The planning or delivering of programs or services; The allocation of resources to any program or service provided or funded by the custodian; Obtaining payment or processing, monitoring, verifying or reimbursing health care claims; and For research, provided that specific requirements and conditions are met. A custodian may share personal health information with an agent of the custodian for any of these purposes.
Disclosure
What is a disclosure of personal health information under PHIPA? The term disclose under PHIPA means to release or make available personal health information that is under the control or custody of a health information custodian, or its authorized agent, to another custodian, individual or organization. It does not include providing information directly back to the person who provided it in the first place, whether or not the information has been altered, so long as it does not include additional identifying information.
What are the rules regarding the disclosure of personal health information? As a general rule, consent is required to disclose an individuals personal health information unless PHIPA allows the disclosure without consent. A health information custodian and its authorized agents may rely on implied consent for the disclosure of personal health information within the circle of care while providing health care so long as the disclosure is reasonably necessary for the provision of health care and the individual has not expressly stated otherwise. Although PHIPA permits custodians to disclose personal health information in certain limited situations, disclosure is not required, unless it is necessary to carry out a statutory or legal duty.
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Express consent will always be required when personal health information is disclosed by a custodian to a non-custodian; where a custodian discloses to another custodian for a purpose other than for health care; or for marketing, research (unless specific conditions are met); and fundraising (if more than contact information is provided). When disclosing personal health information, the custodian should take care to ensure that no information is inadvertently disclosed to third parties.
What are the exceptions to the rules regarding the disclosure of personal health information? PHIPA recognizes the need for a flexible approach to regulating information exchanges between health information custodians in order to ensure the effective and efficient operation of the health system. As such, custodians may disclose personal health information without an individuals consent in certain circumstances, including the following: If the disclosure is reasonably necessary for providing health care and the consent cannot be obtained in a timely manner, unless there is an express request from the individual instructing otherwise; In order for the Minister of Health and Long-Term Care to provide funding to the custodian for the provision of health care services; For the purpose of contacting a relative or friend of an individual who is injured, incapacitated, ill or unable to give consent personally; To confirm that an individual is a patient or resident in a facility or to confirm the status of his/her health condition, unless there is an express request from the individual instructing otherwise; To identify an individual who is deceased or in order to allow a spouse, partner or relative of a deceased person to make decisions about his or her own care or the care of children or to inform estate trustees of an individuals death; To eliminate or reduce a significant risk of serious bodily harm to any person or the public; When transferring records to a custodians successor or to the archives for conservation; For the purpose of carrying out an inspection, investigation or similar procedure that is authorized by a warrant, PHIPA or another Act;
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For determining or verifying eligibility for publicly funded health care or related benefits upon the request of the Minister of Health and Long-Term Care; For the purpose of administration and enforcement of various Acts by the professional Colleges and other regulatory bodies; To a prescribed person listed in the regulations that compiles and maintains a registry of personal health information for the purpose of improving the provision of health care or that relates to the storage or donation of body parts or bodily substances, namely: Cardiac Care Network of Ontario (the registry of cardiac services); INSCYTE (CytoBase); London Health Sciences Centre (Ontario Joint Replacement Registry); and Canadian Stroke Network (Canadian Stroke Registry); To a prescribed entity for the purpose of analysis or compiling information with respect to the management, evaluation or monitoring of the health system, including: Cancer Care Ontario; Canadian Institute for Health Information; Institute for Clinical Evaluative Sciences; and Pediatric Oncology Group of Ontario; To a health data institute for the purposes of health planning and management of the health care system; To the Public Guardian and Trustee, Childrens Aid Society and the Childrens Lawyer for the purpose of carrying out their statutory functions; To a person conducting an audit or reviewing an accreditation or application for accreditation related to the services of a custodian; To a medical officer or a public health authority as required for the purposes of the Health Protection and Promotion Act, for example, to report a communicable disease; For the purpose of legal proceedings if the information is, or relates to, a matter at issue; For the purpose of research, subject to restrictions and conditions; and For any purpose as required or permitted by law.
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Can a health information custodian disclose personal health information to the Workplace Safety and Insurance Board (WSIB) about an injured worker without the individuals consent?
Yes. PHIPA permits the disclosure of personal health information without consent if permitted or required by another law. This means that PHIPA does not interfere with the Workplace Safety and Insurance Act where that Act requires a health practitioner to provide the injured worker, the employer and the WSIB information relating to an employees health care or functional abilities. However, anyone relying on the disclosure provisions of another Act must be mindful that there may be further requirements with respect to the confidentiality of such reports.
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Can personal health information be collected, used or disclosed for marketing purposes?
A health information custodian can only collect, use or disclose personal health information about an individual for market research or for marketing purposes with the express consent of the individual. Note that the following activities are excluded from the definition of marketing: Blood donor recruitment by the Canadian Blood Services; and Communications by health care practitioners about the availability of non-OHIP covered charges for a block fee.
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Research
What are the requirements for the collection, use and disclosure of personal health information for health care research?
In recognizing the importance of health research, PHIPA permits the use or disclosure of personal health information for research purposes without an individuals consent if strict conditions are met. For example, a custodian who uses personal health information for research and, similarly, a researcher who seeks disclosure of personal health information for research, must both submit a detailed research plan to a Research Ethics Board (REB) for approval. In reviewing a research proposal involving the use and disclosure of personal health records, a REB must consider: Whether the research cannot be reasonably accomplished without access to the information; The public interest in conducting the research and in protecting privacy; Whether obtaining consent directly is impracticable; and Whether adequate safeguards are in place to protect the privacy of individuals and the confidentiality of their information. A researcher requesting disclosure of personal health information from a custodian must submit to the custodian a written application, a research plan and a copy of the decision approving the research plan by the REB. In addition, the custodian must enter into an agreement with the researcher that may impose further restrictions on the manner in which the researcher may use and disclose the information. A researcher with an approved research plan who receives personal health information from a custodian shall: Comply with the conditions imposed by the REB, if any; Use personal health information only for the purpose set out in the research plan; Not publish information in a form that could identify the individual; Not disclose information unless required by law or to prescribed entities or registries;
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Not attempt to contact the individual whose personal information is the subject of the research project unless the custodian obtains the consent of that individual; and Notify the custodian in writing of any breaches of either the agreement or PHIPA. Researchers are permitted to disclose personal health information to another researcher or to a prescribed registry or entity if the disclosure is either part of a research plan approved by an REB or it is necessary for the purpose of verifying or validating the information held by the researcher. Researchers who were in possession of personal health information and who lawfully obtained the information from a custodian prior to Nov. 1, 2004 may continue using and disclosing the information for three years after that date.
Are there any requirements for research ethics boards and research plans?
Yes. The regulations specify that a research ethics board (REB) must have at least five members, including: A member who has no affiliation to the person who established the REB; A member who has knowledge in privacy issues; A member who has knowledge in research ethics; and At least two members with expertise in the methods or the relevant areas of research. In addition, the regulations list a number of requirements that research plans must include. For example, a research plan must include a description of why consent to the disclosure of personal health information is not being sought from the individual to whom the information relates; a description of how the information will be used; the safeguards the researcher will put in place to protect the confidentiality and security of the information; and a description of all persons who will have access to the information.
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For instance, an employer may allow an employee to voluntarily provide his or her health card in order to expedite the provision of health care services in the event of an emergency. Please note that any such disclosure must be voluntary, and non-custodians may not require the production of health cards. It is an offence under PHIPA for any organization to wilfully collect, use or disclose any personal health information including health card numbers in a manner that contravenes PHIPA. Likewise, an individual may voluntarily provide his/her health card to a library in order to confirm his/her identity and in order to obtain a library card.
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How long does a health information custodian have to respond to an individuals request for access to personal health information?
A health information custodian must respond no later than 30 days after the request was made. Extensions beyond this 30-day time frame are allowed where meeting this time frame would interfere with the custodians operations, or where outside consultations are required in order to comply with the request. In such situations, the custodian must inform the individual in writing about the delay and the reasons for the delay.
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Can a health information custodian refuse to provide access to an individuals personal health information?
Generally, health information custodians are responsible for assisting individuals by providing access to their health records. Custodians may only refuse access in limited situations, including: The information in question is subject to a legal privilege; Its disclosure could reasonably be expected to result in a risk of serious bodily harm to a person; The information was collected as part of an investigation; or Another law prohibits the disclosure of that information. If any exception applies, PHIPA permits custodians to remove some of the information to allow partial access to the individual. If a health information custodian denies an individual access to his/her personal health information, the individual has the right to file a complaint with the IPC.
Can an individual obtain access to his/her personal health information from a health information custodian who works for a non-health information custodian?
Yes, if the non-health information custodian is not covered by public sector access and privacy legislation. The request would be made directly to the health information custodian.
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What if the health information custodian works for a non-health information custodian that is covered under public sector access and privacy legislation, such as a school board or municipality?
In that case, the individual would submit an access request under the Freedom of Information and Protection of Privacy Act (which covers provincial ministries and most provincial boards, agencies and commissions) or the Municipal Freedom of Information and Protection of Privacy Act (which covers local government organizations such as municipalities, police, school, health and library boards) directly to the freedom of information co-ordinator of the nonhealth information custodian. This does not mean, however, that an individual cannot make an access request directly to the health information custodian, who presumably, would take the necessary administrative steps to obtain it from the freedom of information co-ordinator.
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Can a health information custodian refuse to correct an individuals personal health information?
A health information custodian is obligated to correct personal health information where an individual demonstrates, to the satisfaction of the custodian, that the record is in fact inaccurate or incomplete and the individual gives the custodian the necessary information to correct the record. However, a custodian may refuse to correct personal health information that was not created by the custodian or that is a professional opinion or an observation of a health care provider. If a correction is refused on such a basis, the custodian is required to inform the individual of the refusal, the reasons for the refusal, the individuals right to file a complaint regarding the refusal to the IPC and the right of the individual to attach a statement of disagreement to the record.
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