Michigan Compiled Laws
368-1978-2-26 - Part 26 Data, Information, and Research (333.2601...333.2692)
Section 333.2682 - Statewide Network of Cord Blood Stem Cell Banks.

Sec. 2682.
(1) If funding is made available, the department shall establish a statewide network of cord blood stem cell banks. The director of the department shall enter into contracts with qualified cord blood stem cell banks to assist in the establishment, provision, and maintenance of the network.
(2) A cord blood stem cell bank is eligible to enter the network and be a donor bank if it satisfies each of the following:
(a) Has obtained all applicable federal and state licenses, accreditations, certifications, registrations, and other authorizations required to operate and maintain a cord blood stem cell bank.
(b) Has implemented donor screening and cord blood collection practices adequate to protect both donors and transplant recipients and to prevent transmission of potentially harmful infections and other diseases.
(c) Has established a system of strict confidentiality to protect the identity and privacy of patients and donors in accordance with existing federal and state law and consistent with regulations promulgated under the health insurance portability and accountability act of 1996, Public Law 104-191, for the release of the identity of donors, recipients, or identifiable records.
(d) Has established a system for encouraging donation by an ethnically and racially diverse group of donors.
(e) Has developed adequate systems for communication with other cord blood stem cell banks, transplant centers, and physicians with respect to the request, release, and distribution of cord blood units nationally and has developed such systems, consistent with the regulations promulgated under the health insurance portability and accountability act of 1996, Public Law 104-191, to track recipients' clinical outcomes for distributed units.
(f) Has developed an objective system for educating the public, including patient advocacy organizations, about the benefits of donating and utilizing cord blood stem cells in appropriate circumstances.
(3) A donor bank that enters into the network shall do all of the following:
(a) Acquire, tissue-type, test, cryopreserve, and store donated units of human cord blood acquired with the informed consent of the donor, in a manner that complies with applicable federal regulations.
(b) Make cord blood units collected under this section, or otherwise, available to transplant centers for stem cell transplantation.
(c) Allocate up to 10% of the cord blood inventory each year for peer-reviewed research. This quota may be met by using cord blood units that did not meet the cell count standards necessary for transplantation.
(4) A board of directors shall govern and administer the state cord blood stem cell bank network. The board shall be appointed by the director and consist of members who represent each of the following:
(a) Cord blood stem cell transplant centers.
(b) Physicians from participating birthing hospitals.
(c) The cord blood stem cell research community.
(d) Recipients of cord blood stem cell transplants.
(e) Family members who have made a donation to a statewide cord blood stem cell bank.
(f) Individuals with expertise in the social sciences.
(g) Members of the general public.
(h) Each network donor bank.
(5) Except as otherwise provided under this subsection, each member of the board shall serve for a 3-year term and may be reappointed for 1 or more additional terms. Appointments for the initial members shall be for terms of 1, 2, and 3 years, respectively, so as to provide for the subsequent appointment of an equal number of members each year. The board shall elect a chairperson and do each of the following:
(a) Ensure that the donor banks within the network meet the requirements of subsection (2) on a continuing basis.
(b) Encourage network donor banks to work collaboratively with other network donor banks and encourage network donor banks to focus their resources in their respective local or regional area.
(c) Designate 1 or more established national or international cord blood registries to serve as a statewide cord blood stem cell registry.
(d) Coordinate the donor banks in the network.
History: Add. 2006, Act 637, Imd. Eff. Jan. 4, 2007 Popular Name: Act 368

Structure Michigan Compiled Laws

Michigan Compiled Laws

Chapter 333 - Health

Act 368 of 1978 - Public Health Code (333.1101 - 333.25211)

Article 2 - Administration (333.2201...333.3625)

368-1978-2-26 - Part 26 Data, Information, and Research (333.2601...333.2692)

Section 333.2601 - Applicability.

Section 333.2602 - Meanings of Words and Phrases; General Definitions and Principles of Construction.

Section 333.2603 - Definitions; D.

Section 333.2607 - Definitions; R, S.

Section 333.2611 - Coordination of Activities; Establishment of Policy; Interests to Be Considered; Establishment, Purpose, and Powers of Nonprofit Corporation.

Section 333.2612 - Nonprofit Corporation; Establishment; Purpose; Duties; Selection and Composition of Board of Directors; Appointment and Composition of Internal Management Committee.

Section 333.2613 - Nature of Data to Be Defined by Rule.

Section 333.2614 - Duties of Department Generally.

Section 333.2615 - Level of Coverage; Determination.

Section 333.2616 - Comprehensive Health Information System; Establishment; Provisions.

Section 333.2617 - Comprehensive Health Information System; Statistics.

Section 333.2617a - Maternal Death; Submission of Information for Inclusion in Health Information System.

Section 333.2618 - Publications; Annual Report; Summary Report; Statement of Limitations of Data Used.

Section 333.2619 - Cancer Registry; Establishment; Purpose; Reports; Records; Rules; Medical or Department Examination or Supervision Not Required; Contracts; Evaluation of Reports; Publication of Summary Reports; Commencement of Reporting; Effective...

Section 333.2621 - Comprehensive Policy for Conduct and Support of Research and Demonstration Activities; Conducting and Supporting Demonstration Projects and Scientific Evaluations.

Section 333.2623 - Publication and Dissemination of Results and Information Obtained Under MCL 333.2621.

Section 333.2624 - Grants and Contracts to Conduct or Support Research Activities and Scientific Evaluations.

Section 333.2631 - Data Concerning Medical Research Project; Confidentiality; Use.

Section 333.2632 - Data Concerning Medical Research Project; Inadmissible as Evidence; Exhibition or Disclosure.

Section 333.2633 - Data Concerning Medical Research Projects; Liability for Furnishing.

Section 333.2635 - Power to Demand or Require Data.

Section 333.2637 - Procedures Protecting Confidentiality and Regulating Disclosure of Data and Records.

Section 333.2638 - Violation; Penalty.

Section 333.2639 - Review of Personal Records Upon Request; Procedures for Reviewing Request; Administrative Hearing; Records of Requests.

Section 333.2640 - Parentage Registry; Use and Access by Family Independence Agency; Access to Child's Medical Records and Information; Immunity; Exception.

Section 333.2641 - Fees; Disposition of Collections.

Section 333.2651 - Repealed. 2006, Act 301, Imd. Eff. July 20, 2006.

Section 333.2652 - Receiving and Allocating Bodies or Parts; Purpose; Records of Receipt and Disposition; Universities Designated to Perform Duties and Responsibilities; Powers.

Section 333.2653 - “Unclaimed Body” Defined; Notice to Persons With Authority to Control Disposition of Unclaimed Body; Availability of Unclaimed Body to Department; Request for Notification Concerning Unclaimed Body; Time, Manner, and Contents of No...

Section 333.2655 - Embalming and Disposing of Unclaimed Body; Standards; Holding Period; Identification and Claim by Person With Authority Over Body.

Section 333.2656 - Receiving Unclaimed Body for Educational Purposes; Expense; Record; Disposition.

Section 333.2658 - Postmortem Examination of Unclaimed Body; Certification of Body Unfit for Scientific or Education Purposes; Interment of Unclaimed Body; Expense.

Section 333.2659 - Adoption of Standards for Unclaimed Bodies or Parts.

Section 333.2661 - Repealed. 2006, Act 301, Imd. Eff. July 20, 2006.

Section 333.2663 - Violations; Misdemeanor.

Section 333.2671 - Public Health and Welfare Dependent on Humane Use of Animals for Certain Purposes.

Section 333.2672 - Animal Research Advisory Board; Creation; Membership.

Section 333.2673 - Animal Research Advisory Board; Powers.

Section 333.2674 - Administration of MCL 333.2671 to 333.2675; Expenses of Members.

Section 333.2675 - Inspection of Premises or Property on Which Animals Kept for Experimental Purposes; Purpose.

Section 333.2676 - Registration for Humane Use of Animals for Experimental Purposes; Compliance With Standards; Grounds for Suspension or Revocation of Registration; Findings of Fact Conclusive; Application for Review of Questions of Law; Orders.

Section 333.2678 - Rules.

Section 333.2681 - Definitions.

Section 333.2682 - Statewide Network of Cord Blood Stem Cell Banks.

Section 333.2683 - Educational Materials on Uses and Benefits of Cord Blood Stem Cells; Development and Dissemination; Availability.

Section 333.2683a - Statewide Network of Cord Blood Stem Cell Banks; Public Awareness Efforts; Report on Expenditure of Funds.

Section 333.2685 - Use of Live Human Embryo, Fetus, or Neonate for Nontherapeutic Research; Prohibitions; Presumption.

Section 333.2686 - Diagnostic, Assessment, or Treatment Procedures Not Prohibited.

Section 333.2687 - Embryo, Fetus, or Neonate Considered Live.

Section 333.2688 - Research on Dead Embryo, Fetus, or Neonate; Consent of Mother; Presumption; Authorized Transfer to Medical Research Facilities; Research Standards.

Section 333.2689 - Abortion; Consideration.

Section 333.2690 - Selling, Collecting Fee For, Transferring, Distributing, or Giving Away Embryo, Fetus, or Neonate; Financial Benefit or Compensation Prohibited; Exception; Definitions.

Section 333.2691 - Violation; Penalty.

Section 333.2692 - “Nontherapeutic Research” Defined.