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Policy and Advocacy

2010 FPA Legislative Program

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Written by Michael A. Jackson29
Monday, 31 May 2010 12:21
Last Updated (Monday, 31 May 2010 15:29)

2010 Florida Pharmacy Association Legislative Program

At the heart of professional organizations is the need to provide input to state and federal policy makers. The Association wishes to give thanks our legislative consultants Lori Weems, Manny Prieguez and their staff for their tireless efforts to work our issues before the House, Senate, Board of Pharmacy and Governor’s Office. In the past our policy work has concentrated on the Florida legislature and various state agencies that regulate the profession and business of pharmacy. Perhaps the most compelling issue that we found in this election year is the host of bills that were filed that were not approved. This is not unusual given the upcoming election season with a large candidate pool and incumbents seeking re-election. As we go to press with this report the Governor had not signed most of the legislation that passed. We should have more current information available at the annual meeting.

On occasion members may ask why the FPA continues to monitor issues with Medicare and Medicaid. It is very important that we all understand how pharmacy services are reimbursed. In Florida this state will spend $8 billion providing health care access to the 2.7 million citizens of this state that are Medicaid eligible. The Federal government will kick in an additional $11 billion. If you look at Medicaid and Medicare it is quite obvious that the largest payer of pharmacy services is state and Federal governments. Major policy decisions in both those arenas have a very significant impact on many sectors of our industry.

This year the FPA traveled to Washington, DC on several occasions to ensure that efforts to reform health care included a viable place for our profession. Hill visits were performed by FPA members and leadership under the guidance of NACDS, NCPA and APhA. While the final legislation that Congress approved is not perfect a number of corrections to pharmacy issues were included in the health care reform bill that passed.

For a detailed report on the 2010 legislative session as well as other advocacy issue enter here.


 

Technician Registration Form on BOP Web Site

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Written by Michael A. Jackson29
Tuesday, 21 July 2009 00:00
Last Updated (Wednesday, 23 June 2010 13:51)

The Florida Board of Pharmacy has been in rule development since passage of Senate bill 1360 during the 2008 legislative session. This bill requires pharmacy technicians to register with the Florida Department of Health. Other issues in the legislation include the following:

Requires the Board of Pharmacy to adopt rules on registration
Requires registered technicians to be 17 years old
Requires 20 hours of CE (4 hours live, 2 hours med errors)
Registration must be available to the public as well as board inspectors
Pharmacy interns exempt from registration
Technician students exempt from registration
Pharmacist with discipline not eligible to register as technician
 




By January 1, 2011 Registered Technicians must have:
  • Completed a Board approved training program or
  • Have completed a certification program approved by NCCA or
  • Have worked a minimum of 1,500 under a licensed pharmacist
The FPA has been informed by the Department of Health that technician registration will begin around the 1st of October.   Technicians will have until December 31st to register.  An on-line application is available through the Board's web site (ENTER HERE).  We do not know at this time what that application will look like. Technicians will need to be able to demonstrate that they have completed one of the three registration requisites by the end of next year (2010).  The Florida Department of Health is also making available a way for employers to apply for an "other payer code" if they plan to proactively register their pharmacy technicians.  Information on how to do that can be found through this link under "Other Payer Code Information".

For a list of frequently asked questions from the Department of Health enter here.

FOR TRAINING PROGRAM RULE DRAFT SEE BELOW

Read more: Technician Registration Form on BOP Web Site

 

RxPatrol

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Written by Michael A. Jackson29
Friday, 30 January 2009 20:14
Last Updated (Friday, 30 January 2009 21:59)

The Florida Pharmacy Association recognizes the need for collaboration between the pharmaceutical industry, law enforcement and professional organizations. The FPA is working with Purdue Pharma and RxPatrol.org to help create public awareness from within the pharmacist community with drug related crimes. According to the RxPatrol web site, Florida is one of the top 10 states in terms of robberies and burglaries. It is clear that work is needed in this area to address the rising tide of pharmacy crimes.
 
Consider the following:
Since June of 2008, RxPATROL is credited with 56 arrests for pharmacy crimes.

RxPATROL is a collaborative effort between industry and law enforcement designed to collect, collate, analyze and disseminate pharmacy theft information. RxPATROL helps protect the pharmacy environment and ensure legitimate patients' access to life-sustaining medicines.  For information on how to get involved or download resources visit www.rxpatrol.org.
   

Methamphetamine Training Resource

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Written by Michael A. Jackson29
Wednesday, 24 December 2008 12:28
Last Updated (Monday, 29 November 1999 19:00)

Required Training for Retailers of Ephedrine, Pseudoephedrine and Phenylpropranolamine


The Combat Methamphetamine Epidemic Act of 2005 (Title VII of the USA PATRIOT Improvement and Reauthorization Act of 2005, P.L. 109-177) was signed into law March 9, 2006. All changes went into effect on March 9, 2006, (date the legislation was signed). The Combat Methamphetamine Epidemic Act primarily affect persons selling products containing the List I chemicals ephedrine, pseudoephedrine, and phenylpropanolamine.  This act directs businesses to train staff and certify with the Federal goverment that this training has taken place.  The Office of Diversion Control on the DEA website.

DEA has developed training materials regarding self-certification training for regulated sellers of non-prescription drug products containing ephedrine, pseudoephedrine, and phenylpropanolamine as required by the Combat Methamphetamine Epidemic Act of 2005.  You can download those training materials from the above web site link.  We understand this there may be a requirement for training to take place on an annual basis along with the obligation to recertify with the U.S. Department of Justice

Self-Certification and Training

(1) Seller must self-certify to the Attorney General that each individual who is responsible for delivering such products into the custody of purchasers, or who deals directly with purchasers by obtaining payment for the products, has undergone training provided by the seller to ensure that the individual understands the requirements that apply to the sale of these products.

(2) Regulated seller may not sell any scheduled listed chemical product at retail unless the self-certification has been submitted to the Attorney General.

(3) Seller must maintain a copy of such self-certification and records demonstrating that individuals have undergone such training.

(4) The certification is not effective unless, in addition to provisions regarding the training of individuals, the certification includes a statement that the seller understands each of the requirements regarding transactional limits, blister-packs, "behind the counter" placement, photo identification, and logbook also apply and agrees to comply with the requirements.

(5) The Attorney General will issue regulations to establish the criteria for self-certifications and employee training. Separate certification is required for each place of business at which a regulated seller sells such products at retail.

(6) The Attorney General will establish a program that will:

(a) be carried out through an Internet site of the Department of Justice;

(b) inform regulated sellers that 18 U.S.C. § 1001 applies to such certifications;

(c) make available to sellers the criteria for certification and training;

(d) be designed to permit submission of certifications through the Internet site; and

(e) be designed to automatically provide the explanation of the criteria for certification and training and an acknowledgment that the Department of Justice has received a certification, without requiring direct interaction of regulated sellers with staff of the Department of Justice.

(7) Copies of certifications shall be made available to appropriate State and local officials.

 

2008 Legislative Program

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Written by Michael A. Jackson29
Sunday, 28 September 2008 20:10
Last Updated (Sunday, 28 September 2008 20:37)

110-1029_img.jpg The FPA advocacy program for the 2008 legislative session included a review of pharmacist technician regulations, requirements for pharmacists to dispense contraceptive products and restrictions on pharmacists ability to enterchange generic drugs.  Also included in this year's session was a significant revision on licensure transfer regulations for pharmacists wishing to practice in this state.

The Association will be conducting several law conferences to recap all of these activities.  Visit our "Upcoming CE Conferences" section of our web site for more information.

Alex Pytlarz, Legislative Committee Chair
Michael Jackson, R.Ph. Executive Vice President and CEO
   

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