Describe both the general responsibilities of compounding personnel and those specific to the. Usp chapter 797, and apply them in a variety of nuclear pharmacy practice settings. Usp 800 is the latest united states pharmacopeia usp revision which clarifies and expands upon hazardous drug compounding both sterile and nonsterile. At the end of the general compounding domain, you will be asked if you want to answer questions for usp.
Kastango, mba, rph, fashp the top 10 gaps in usp chapter compliance understand regulation assess risk level develop action plan implement compliance plan control measure communicate ve state of compliance point in time figure 1. About notice 797, possible federal tax refund due to the. The usp received appeals on specific provisions of the chapter, and those appeals were subsequently granted, effectively sending this version of the chapter back to the expert committee. Usp sets standards for the quality of drug products and works with healthcare providers to help them meet the standards.
Department of the treasury internal revenue service notice 797. Mar 18, 2015 usp chapter, pharmaceutical compounding. Vigorous hand washing with antimicrobial soap for 2 minutes up to the elbows before donning gloves. The compounding expert committee of usp began a new set of revisions in july 2010, and on september 25, 2015, usp issued a set of proposed revisions to usp 797 for public comment. Pharmacy rulesregulations by state for compliance with usp 797. Shoe covers, head and facial hair covers, face masks, tyvek nonshedding gown and sterile gloves required. State oversight of drug compounding pdf the pew charitable. Sterile preparations, became effective january 1, 2004 6. As a result, in march 2014, usp published a proposed set of guidance known as usp that dealt with hd handling in health. The revised section on environmental monitoring discusses requirements. Meaningful quality standards are important for all forms of compounded drugs.
Identify the key acronyms and state the definition of key terms associated with usp. If you are eligible, claim the eic on your 2015 income tax return. Proposed revisions to usp 797 overview and current status. General chapter 797, pharmaceutical compounding sterile preparations usp, the latest version of which was issued in 2008. This discussion guide is a followup to a discussion guide that was developed when the original chapter became official.
Although usp provides guidelines for preparing sterile compounds. Proposed revision to usp chapter 797 for sterile compounding will be published for comment on november 2, 2015 and comments will be accepted until january 31, 2016. Your home, and your spouses if filing a joint return, was in the united states for over half of 2010. Compliance to usp 797 regarding pharmacy compounding is an ongoing and increasingly important issue for all compounding pharmacies to address as quickly as possible. In accordance with the rules and procedures of the 20152020 council.
Usp 795 and usp 797 compliance are not as frequently talked about recently, yet they are as important as ever. Iso classification of particulate matthalmic drops and ointments, and tissue ter in room air limits are in particles of 0. Usp chapter 797 general overview personnel cleansing and garbing requirements. Office of manufacturing qualityoffice of compliance. Usp chapter gap analysis page 6 of 16 x medical center confidential and proprietary for internal use only entry door. September 23, 2019 revised general chapter is postponed until further notice. Proposed revisions to usp chapter 797 for sterile compounding date.
Included among usps standards are those related to the practice and quality standards for compounded sterile preparations, usp 797. Sterile compounding webinar california hospital association. Revision status of usp chapter 797 pharmaceutical compounding. Although the us pharmacopeial convention usp addressed hds in a 2008 update to usp for the issue of compounding sterile parenteral hds, the update fell short due to a lack of guidance for nonparenteral products. Some facility requirements will necessitate a revision to usp 797.
The return is located in the in the ceiling the back of the room away from the entry door. Blueprint for implementing chapter 797 for compounding. Information about notice 797, possible federal tax refund due to the earned income credit eic, including recent updates, related forms, and instructions on how to file. D uring the 1960s, the practice of pharmacy began growing and evolving. March 12, 2020 appeals panel issues decisions on the appeals to usp, and see faqs on usp compounding appeals. Notice 797 informs the public that they may be eligible for a refund on their federal income tax return because of the earned income credit eic. Uspnf establishes standards for medicines, food ingredients and dietary supplements.
Usp chapter, and apply them in a variety of nuclear pharmacy practice settings. Usp 797 pharmaceutical compoundingsterile preparations. All rights reserved 21 i would like to comment on the hazardous drugs as csp. Sterile preparations, was released in late 2007 and will become official on june 1, 2008. Possible federal tax refund due to the earned income. Pharmasystems solutions for usp compliance sterile preparations for compounding pharmacies usp chapter, sterile preparations for pharmaceutical compounding, details the quality standards, conditions and procedures for compounding sterile preparations csps of drugs and nutrients in a cleanroom. Usp chapter general overview personnel cleansing and garbing requirements. The benefits of usp 797 compliance include the minimization of contamination of csps, improved aseptic proficiency of hospital pharmacy personnel. General chapter usp establishes best practices and regulations for the production of compounded sterile preparations. Compounding sterile preparations 1 t he revision bulletin to usp chapter 797, pharmaceutical compounding. Sterile compounding inspection requirements please use this document to prepare for your sterile compounding.
Ever since the 2012 meningitis outbreak that had been linked to the now defunct new england compounding center necc, increased legislation is constantly being introduced. Chapter 797 is a pharmaceutical compounding document produced by the united states pharmacopeia usp. The significant progress in adopting usp chapter quality standards and. Iso classification of particulate matthalmic drops and ointments, and tissueter in room air limits are in particles of 0.
Some facility requirements will necessitate a revision to usp. Pharmaceutical compounding sterile preparation, united stated pharmacopeia 36national formulary 31. If you answer yes then you will not be presented with any usp 797 questions. Wa pharmacy quality assurance commission 2020 responsible. Usp seeks feedback on american pharmacists association. Low air returns, unless smoke studies prove compliance. Pharmaceutical compoundingsterile preparations revision bulletin table 1. Chapters 1 through 999 are enforceable standards that describe how certain functions and processes are to be performed. Identify the key acronyms and state the definition of key terms associated with usp 797. Thus, their testing procedures must be verified to meet the usp requirements stated in the individual monograph for the component being tested. Iso classification of particulate matter in room air limits are in particles of 0. The usp 797 gap tool has been updated to reflect the version of usp general chapter 797 that was published on june 1, 2020.
Establishing a practice standard for compounding sterile preparations in pharmacy find, read and cite all the research. Usp 797 compliance with usp 797 is our duty because. Air returns in the cleanroom suite must be low on the wall unless a. Pharmaceutical compoundingsterile preparations notificaton. Kastango, mba, rph, fashp dont just know about it these changes may have a significant impact on the daytoday practices of all persons involved in the handling, preparation, and storage of csps. Interested parties may submit comments by mail or commercial carrier by august 15 to. The existing chapter had provided procedures for allergen immunotherapy extracts as a separate element to processes applicable to three levels of risk for other sterile compounded products. Usp chapter 797 gap analysis page 6 of 16 x medical center confidential and proprietary for internal use only entry door. It is no longer acceptable for facilities that prepare a low number of hds to use a biologic safety cabinet bsc or a compounding aseptic containment isolator caci in a nonnegative pressure room. After publication of the revised on june 1, 2019, usp received appeals on certain provisions of the. Pharmaceutical compoundingsterile preparations uspnf. In september 2015, the united states pharmacopeia usp released a proposed updated chapter 797 on procedures for sterile compounding. Pharmacopeia 12601 twinbrook parkway rockville md 208521790.
For example, under dextrose injection, the following is stated. Oct 27, 2015 proposed revision to usp chapter 797 for sterile compounding will be published for comment on november 2, 2015 and comments will be accepted until january 31, 2016. October 20, 2015 proposed revision to usp chapter 797 for sterile compounding will be published for comment on november 2, 2015 and comments will be accepted until january 31, 2016. Overview of chapter for surveyors and inspectors kate douglass october 9, 20. However, a requirement statement from usp has been added in blue. Pdf on oct 1, 2004, eric s kastango and others published usp chapter 797. In 2015, representatives from nearly twothirds of state boards of pharmacy that. There is no record of room particle counts for estimation of room cleanliness.
Apr 18, 2019 usp 797 hazardous cleanroom design usp 800 while usp 797 previously established requirements for hazardous drug compounding, usp chapter 800 sets forth new requirements. Usp 797 sterile compounding study guide flashcards quizlet. Guidelines for pharmaceutical sterile preparations chapter 797. To help ensure clarity and consistency, the faqs are being revised. Establishing a practice standard for compounding sterile preparations in pharmacy find, read and cite all. Usp 797 is a farreaching regulation that applies to health care institutions, pharmacies, physicians practice facilities, and other facilities in which compound sterile preparations are prepared, stored, and dispensed. Based on the number and significance of public comments received in response to the. These tools can help build the foundation for a corrective action plan that details the activities and resources needed to comply with usp compounding requirements. Pharmasystems solutions for usp compliance sterile. It is now five years since the new england compounding center necc tragedy brought compounding specialty pharmacies to the attention of the media and the us public. The last official revision to usp 797 became official on june 1, 2008.
Originally written in 2004, chapter 797 is popularly agreed to increase the safety of the compounding setting and its ingredients. It improves the health and wellbeing of our patients and 2. You can return at any point and change your answer to no and the hidden domains will be available. Apr 01, 2015 usp is designed to complement both usp and usp 797. Understanding usp 797 conclusion the current usp 797 regulations emphasize the need to maintain highquality standards for processes, components, and environments for sterile compounding preparations. Usp 797 clean room guidelines standards for sterile. See your 2010 income tax return instructions for more details. Understanding usp chapter 797 engineering control certification requirements and environmental sampling and remediation strategies chs pharmacy education series proce, inc. Compliance with usp chapter 797 was added as a requirement on october 30, 2015 language added to the pharmaceutical services section to require compliance with usp chapter 797 when compounding sterile preparations language added to the nursing services section to require compliance with. Completely reorganizes the chapter and groups like sections together, eliminating redundancies, and clarify requirements. Brief history of usp 797 and the current, proposed revisions. Usp 797 hazardous cleanroom design usp 800 while usp 797 previously established requirements for hazardous drug compounding, usp chapter 800 sets forth new requirements. In response to an increasing number of patient injuries due to medication delivery and sterile compounding, the industry began calling attention to safety.