In a presentation prepared for a meeting Wednesday of the
Maria Millan CIRM photo |
Millan said patients are being harmed by unproven treatments at clinics in California and elsewhere. The chairman of the board of her agency, Jonathan Thomas, has called the treatments "snake oil." (The agency is formally known as the California Institute for Regenerative Medicine (CIRM).)
A small task force of the State Board is laying the groundwork for additional regulation of the industry, which has grown rapidly in recent years. Estimates are that 1,000 clinics exist across the country with the largest number in California.
Earlier this year, a measure to set standards for the clinics died in a legislative committee. The board itself initiated its task force more than a year ago. This week is its first public hearing.
Millan's slide presentation for the meeting did not go into details. But she called for improved informed consent from patients and raised the following considerations:
- Creation of publicly available registries of stem cell treatment options
- Creation of a method for patients to self-report outcomes or harm from unregulated regenerative medicine treatments
- Requiring "clear visibility" for patients of the treatment team's credentials
- Creation of a "mechanism for investigating those holding healthcare licenses suspected of violating professional standards when providing unproven stem cell interventions, particularly those outside their scope of training"
- Registration of treatments that involve human cellular and tissue products along with a clear distinction between federallly authorized treatments and practice of medicine
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