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So far Michael Angeloni has created 903 blog entries.

West Virginia

At the Board of Pharmacy’s recent meeting, the Board voted to release a statement regarding the Third Amendment to the Federal PREP Act declaration:  A WV immunizing pharmacist who orders and administers pediatric vaccines in compliance with DHHS’ declaration during the federally-declared COVID-19 public health emergency shall not be deemed by the WV Board of Pharmacy to be in violation of the WV Pharmacy Practice Act or §15-12. The statement also offers a comparison of the requirements of the Federal Law v. WV Law.

Also in WV. The Board of Pharmacy published an emergency rule amending regulations under 15 WVCSR 1 to remove dispensing requirements for chloroquine and hydroxychloroquine established under a previous emergency rule, as the drugs are no longer facing supply shortages. The rule also defines activities that are not “compounding” to distinguish between compounding and combining prescriptions. In addition, the rule allows practitioners 15 days to provide an original prescription for emergency oral prescriptions and specifies acceptable methods for delivery, including electronically. Portions of the rule are in response to the Covid-19 pandemic. The rule is effective on approval by the Secretary of State or October 7, 2020, whichever occurs first.

For more information, contact NACDS’ Jill McCormack at 717-592-8977.

2020-09-04T11:16:57-04:00September 4, 2020|West Virginia|

Wisconsin

A final rule of the Department of Safety and Professional Services, Controlled Substances Board, amends the Prescription Drug Monitoring Program (PDMP) effective September 1. The rule requires drug dosage units and the partial fill indicator to be submitted to the program and clarifies that health care professionals may access PDMP reports for scientific research purposes if the patient is a direct patient and gave informed consent.

For more information, contact NACDS’ Joel Kurzman at 847-905-0555.

2020-09-04T11:15:52-04:00September 4, 2020|Wisconsin|

Arkansas

The Insurance Department posted a notice to announces the issuance of Bulletin No. 29-2020 on the extension of portions of certain coronavirus (COVID-19) bulletins issued under Executive Order 20-03, as amended by executive orders 20-25, -37, and -45 to extend the suspension of the consumer signature requirement for pharmacist services and certain obligations of pharmacy benefit manager (PBM) under the state price-gouging law.  This extension became effective August 14 and will remain for the duration of the public health emergency.

For more information, contact NACDS’ Mary Staples at 817-442-1155.

2020-08-28T11:05:03-04:00August 28, 2020|Arkansas|

California

For the past four months, NACDS jointly with the California Retailers Association, the California Pharmacists Association and Board of Pharmacy, has been urging Governor Gavin Newsom’s Administration to remove existing barriers to allow pharmacies to fully engage in COVID testing. In early May, the Governor granted authority allowing pharmacies to only collect test specimens, due to limited restrictions of requirements to have a laboratory director. Finally, on August 24, the Governor signed an Executive Order increasing the availability of CLIA-waived COVID-19 testing by pharmacies. The order directs the Department of Consumer Affairs, in consultation with the California Department of Public Health, to issue waivers (DCA-20-45) permitting pharmacies with CLIA-waived certificates to have their pharmacists and pharmacy technicians to conduct CLIA-waived COVID-19 tests — order tests, collect specimens, process with the appropriate equipment and quickly provide patients with the results.

Also in California. The Department of Resources Recycling and Recovery has opened the comment period for the third draft of the Pharmaceutical and Sharps Waste Stewardship Proposed Regulations.  The 15-day comment period is opened on August 21 and will close on September 4, 2020.  Written comments can be submitted to pharmasharps@calrecycle.ca.gov.

For more information, contact NACDS’ Mary Staples at 817-442-1155.

2020-08-28T11:04:07-04:00August 28, 2020|California|

Georgia

The Board of Pharmacy will hold a public hearing on the eleven (11) proposed rules and amendments provided here via conference call at its upcoming meeting scheduled for Wednesday, September 16, 2020.  Comments to the proposed amendments are due to the Board by September 9, 2020.

For more information, contact NACDS’ Leigh Knotts at 803-243-7207.

2020-08-28T11:03:00-04:00August 28, 2020|Georgia|

Kentucky

Effective January 1, 2021, the Kentucky Cabinet for Health and Family Services (CHFS) will utilize Version 4.2B of the American Society for Automation in Pharmacy (ASAP) Prescription Drug Monitoring Program Standard for reporting controlled substance data to KASPER. Members may want to take the following actions to prepare:

  • Review the implementation guide for Version 4, Release 2B of the ASAP Prescription Drug Monitoring Program Standard
  • Review the KASPER Controlled Substance Reporting Guide:
  • By Jan. 1, 2021, ensure your pharmacy systems are reporting two newly required fields:
    1. DSP12 Transmission Form of Rx Origin Code.
    2. DSP13 Partial Fill Indicator. CHFS will require this field for all prescription records reported to KASPER.

Additionally,  effective January 1, 2021, when the PAT02 value is 07 for Social Security Number, the vast majority of records, the PAT03 value must be nine numeric digits or the record will be rejected with a fatal error and will need to be corrected.

Lastly, to support EPCS, KASPER will track the DSP20 – Electronic Prescription Reference Number, and DSP21 – Electronic Prescription Order Number fields. Reporting these fields is optional, but KASPER is requesting that pharmacies report this if capable.  For further detail, please contact KASPER administration at (502) 564-2815 or eKASPER.admin@ky.gov.

Also in KY. NACDS reminds members that Kentucky Revised Statute 218A.182 mandates the electronic prescribing of controlled substances (EPCS) effective January 1, 2021. The Kentucky mandate is similar to the federal Medicare Part D EPCS mandate effective January 1, 2021, but applies to all controlled substances prescribed in Kentucky. Click here for more information, including criteria and process for an exemption.

For more information, contact NACDS’ Jill McCormack at 717-592-8977.

2020-08-28T10:59:13-04:00August 28, 2020|Kentucky|

North Carolina

For all pharmacies that have received a Cost of Dispensing Survey response request, North Carolina Medicaid has extended its Cost of Dispensing Survey deadline from August 18th to September 1st.

Also in North Carolina. The Medical Board has issued a proposed rule which would amend regulations under 21 NCAC 32S to remove the physician’s assistant’s license number and authorized primary or back-up physician’s name and telephone number from the required information in the physician assistant prescription. A hearing is scheduled for October 16, 2020, via teleconference. Comments on the proposed rule are also due on October 16, 2020.

For more information, contact NACDS’ Leigh Knotts at 803-243-7207.

2020-08-28T10:56:03-04:00August 28, 2020|North Carolina|

Texas

As two hurricanes headed for the Texas Gulf coast, earlier this week Governor Greg Abbott declared a disaster in multiple counties which automatically triggered emergency procedures for dispensing of medications. Additional information on the declared state of emergency can be found here.

Also in Texas.  The Department of Insurance, Division of Workers’ Compensation issued an emergency rule waiving certain CMS distant site practitioner requirements during the COVID-19 outbreak that would allow health care providers licensed to perform physical medicine and rehabilitation services to bill and receive reimbursement for services allowed under current CMS telemedicine and telehealth billing codes.  Under this emergency rule, these waivers will be extended until October 9, 2020.

Also in Texas. The Health and Human Services Vendor Drug Program (VDP) issued three announcements:

  1. Opioid-Related Clinical Prior Authorization Criteria Updates – VDP regularly updates clinical prior authorization criteria to better align drug policies and prior authorization approval criteria with the latest information available on drug information packets, the federal or state regulations. Opioid-related prior authorizations are scheduled for revision on September 1, 2020, to align with the uniform opioid policy.
  2. Insulin Products Return to Non-Preferred Status – VDP temporarily removed the non-preferred status on April 1 in response to reported drug shortages for insulin products in the “Hypoglycemics, Insulins” drug class. VDP will reverse this change in status because of sufficient availability in the market. Beginning September 18, 2020, the Medicaid formulary will reflect the Preferred Drug List status changes for all non-preferred insulin products.
  3. Inhaled Glucocorticoids Products Return to Non-Preferred Status – VDP temporarily removed the non-preferred status on April 1 in response to reported drug shortages for medications in the “Glucocorticoids, Inhaled” drug class. VDP will reverse this change in status because of sufficient availability in the market. Beginning September 18, 2020, the formulary will reflect the Preferred Drug List status changes for all non-preferred inhaled glucocorticoid products.

Also in Texas. On September 1, 2020, the Health and Human Services Commission (HHSC) will expand the Medicaid and CHIP benefit to allow and reimburse pharmacists for administering certain medications in a pharmacy setting, including the administration of certain long-acting anti-psychotics, opiate dependence treatments and emergency treatment for known or suspected opioid overdoses, and flu vaccines.  Under this benefit, pharmacies must be reimbursed for the ingredient cost, administration fee, and applicable dispensing fee for each claim processed. Pharmacies will also be reimbursed for the administration of flu vaccines for ingredient cost and the administration fee. To prepare pharmacies for changes to the claims submission process an addendum (PDF) to the NCPDP B1 Transaction Billing Request Payer Sheet is available showing changes to three existing fields in the Drug Use Review/Professional Pharmacy Service segment and addition of one new field to the Pricing segment. Pharmacies should refer to the addendum for more information on how this change impact claims processing. VDP will revise the full B1 payer sheet upon implementation. More information can be found here.

For more information, contact NACDS’ Mary Staples at 817-442-1155.

2020-08-28T10:54:46-04:00August 28, 2020|Texas|

Alabama

The Department of Public Health has issued a proposed rule that would amend regulations under AAC 420-7-2 to add tianeptine to the Schedule II list of controlled substances. The rule also would remove Epidiolex® from the list of Schedule V controlled substances. Comments to the proposed rule are due September 4, 2020.

For more information, contact NACDS’ Leigh Knotts at 803-243-7207.

2020-08-21T08:56:27-04:00August 21, 2020|Alabama|
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