Maine Revised Statutes Title 22 Sec. 8735 – Compliance
Current as of: 2023 | Check for updates
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1. Certification of accuracy. A manufacturer, wholesale drug distributor or pharmacy benefits manager that submits a notification or report to the organization pursuant to this subchapter shall submit with the notification or report a signed written certification of the notification’s or report’s accuracy.
[PL 2019, c. 470, §8 (NEW).]
Terms Used In Maine Revised Statutes Title 22 Sec. 8735
- Manufacturer: means an entity that manufactures or repackages, and sets the wholesale acquisition cost for, prescription drugs that are distributed in the State. See Maine Revised Statutes Title 22 Sec. 8731
- Organization: means the Maine Health Data Organization established under this chapter. See Maine Revised Statutes Title 22 Sec. 8702
2. Civil penalty. A manufacturer, wholesale drug distributor or pharmacy benefits manager that violates this subchapter commits a civil violation for which a fine of $30,000 may be adjudged for each day of the violation.
[PL 2019, c. 470, §8 (NEW).]
3. Audit. The organization may audit the data submitted by a manufacturer, wholesale drug distributor or pharmacy benefits manager pursuant to this subchapter. The manufacturer, wholesale drug distributor or pharmacy benefits manager shall pay for the costs of the audit.
[PL 2019, c. 470, §8 (NEW).]
4. Corrective action plan. The organization may require a manufacturer, wholesale drug distributor or pharmacy benefits manager subject to this subchapter to develop a corrective action plan to correct any deficiencies the organization finds with the manufacturer’s, wholesale drug distributor’s or pharmacy benefits manager’s compliance with this subchapter.
[PL 2019, c. 470, §8 (NEW).]
SECTION HISTORY
PL 2019, c. 470, §8 (NEW).