Friday, May 17, 2013

Virginia Board of Health Professions Announces Public Hearing to Receive Comments on Pharmacy Technician Scope of Practice

Following up on last year's Board of Health Professions study of pharmacists, the Board announced on Tuesday, May 14th that they will now move forward with studying the current duties, responsibilities, training and education of pharmacy technicians and will determine what changes, if any, should be made to laws and regulatory policies to best enable effective team approaches for the care of Virginia's patients.

The Board of Health Professions has announced the timetable for the pharmacy technician study:
  • July 30, 2013: Public Hearing/Committee Meeting
  • July-August 2013: Open Public Comment Period
VPhA encourages you to think about your current practice and if there are any unnecessary restrictions that you feel should be altered to ease the burden on pharmacists and pharmacy technician and better ensure access to healthcare through strengthened health professional teams.
The VPhA Board of Directors would like to hear your thoughts and suggestions concerning the review of Pharmacy Technicians.  If you have comments, please feel free to response send us an email at vpha@virginiapharmacists.org.

Thursday, May 16, 2013

USP Prescription Container Labeling Becomes Official Standard

The United States Pharmacopeia (USP)  General Chapter <17>Prescription Container Labeling, published in the USP 36-NF 31, became an official standard on May 1, 2013. The standards, which provide a universal approach to the format, appearance, content and language of instructions for medicines in containers dispensed by pharmacists, were published in General Chapter <17> in November 2012. Visit the National Association of Boardsof Pharmacy Web site for additional information. 


Wednesday, May 8, 2013

Free Archive of Immunization Webinars Posted (No CE Credit Available for Archive)

Unable to attend one of the three webinars hosted by VPhA and the Virginia Department of Health or in need of a refresher of the content?  Archives of all three programs are now available for you to view at your leisure.  Note: CE credit is NOT offered for the archived webinars.

- Immunization Update 2012
- Best Practices for Vaccine Administration and Documentation
- Preventing Hepatitis B Among Diabetics

Archive Viewing (Not Eligible for CE Credit)
To view the archived webcast of the programs:
1. Visit https://lobby.mc.iconf.net/gcc/conferencing/partaccess.asp?ba=6
2. Enter the Moderator's Meeting Number: 4970431
3. Click "View List of Archives" *
4. Select from the list of available archives and click "View"
     - Note: please ignore the "Expired" text after the Immunization Update 2012.  The "view" link is still active.

Planning is already underway for future webinars from VDH and VPhA. Please be on the lookout for future opportunities.

* Some internet browsers do not show the option to click "View List of Archives". If you do not see this option, please try an alternate internet browser such as Internet Explorer.

Friday, January 4, 2013

VPhA Tracking the 2013 Virginia General Assembly Session

With session less than a week away, VPhA has already identified 13 bills that impact pharmacy.  This number will grow over the next 2 weeks as a few thousand bills will be introduced by the 140 members of the Virginia General Assembly.

Work has already begun in amending or defeating negative bills and we are actively working to ensure safe passage of HB1501 which amends the Collaborative Practice language to allow for greater use and flexibility of Collaborative Practice agreements.

To follow along with VPhA's work at the General Assembly, please click here.

(Note: to ensure that you are viewing the most up-to-date bill list, please compare the date and time listed on the document vs the date and time listed on the web page.  If the dates do not match up, we ask that you hit refresh in your internet browser and this should give you the updated bill list document)

Thursday, December 27, 2012

DEA Notice of Proposed Rulemaking: Regulations Governing the Secure Disposal of Controlled Substances by Both DEA Registrants and Ultimate Users.

On Friday, December 21st, the DEA posted a Notice of Proposed Rulemaking for requirements to govern the secure disposal of controlled substances by both DEA registrants and ultimate users.

The proposed regulations would allow retail pharmacies, manufacturers, distributors, reverse distributors to voluntarily administer mail-back programs and maintain collection receptacles (all after obtaining authorization from the DEA to be a "collector"). In addition, this proposed rule expands the authority of authorized retail pharmacies to voluntarily maintain collection receptacles at long term care facilities.

For complete information, including the proposed regulations, please visit: http://www.deadiversion.usdoj.gov/fed_regs/rules/2012/fr1221_8.htm

SUMMARY: This rule proposes requirements to govern the secure disposal of controlled substances by both DEA registrants and ultimate users. These regulations would implement the Secure and Responsible Drug Disposal Act of 2010 (Pub. L. 111-273) by expanding the options available to collect controlled substances from ultimate users for purposes of disposal to include: Take-back events, mail-back programs, and collection receptacle locations. These proposed regulations contain specific language to continue to allow law enforcement agencies to voluntarily conduct take-back events, administer mail-back programs, and maintain collection receptacles. These regulations propose to allow authorized manufacturers, distributors, reverse distributors, and retail pharmacies to voluntarily administer mail-back programs and maintain collection receptacles. In addition, this proposed rule expands the authority of authorized retail pharmacies to voluntarily maintain collection receptacles at long term care facilities. This proposed rule also reorganizes and consolidates existing regulations on disposal, including the role of reverse distributors.

DATES: Electronic comments must be submitted and written comments must be postmarked on or before February 19, 2013. Commenters should be aware that the electronic Federal Docket Management System will not accept comments after midnight Eastern Time on the last day of the comment period.

ADDRESSES: To ensure proper handling of comments, please reference "Docket No. DEA-316" on all electronic and written correspondence. DEA encourages all comments be submitted electronically through http://www.regulations.gov using the electronic comment form provided on that site. An electronic copy of this document is also available at the http://www.regulations.gov Web site for easy reference. Paper comments that duplicate the electronic submission are not necessary as all comments submitted to http://www.regulations.gov will be posted for public review and are part of the official docket record. Should you, however, wish to submit written comments via regular or express mail, they should be sent to the Drug Enforcement Administration, Attention: DEA Office of Diversion Control (OD/DX), 8701 Morrissette Drive, Springfield, Virginia 22152.

FOR FURTHER INFORMATION CONTACT: John W. Partridge, Executive Assistant, Office of Diversion Control, Drug Enforcement Administration; Mailing Address: 8701 Morrissette Drive, Springfield, Virginia 22152; Telephone: (202) 307-4654.