A PCCA Pharmacy Compliance Specialist will conduct an audit of your facility and equipment to determine its compliance with USP <797> and <795>. This assessment is a survey/checklist of systems and documents that according to industry regulations should be in use at your facility. Items on the checklist that are not observed at your facility are considered “gaps” that need to be addressed and corrected in order to ensure your facility, equipment and personnel are compliant with the requirements of <797> and <795>. During this one- to two-day analysis of your facility your PCCA Compliance Specialist will review your:
After this review and observation period, your PCCA Compliance Specialist will spend a half-day generating a final report of conclusions and findings. This report will demonstrate your company’s strengths as well as areas that require improvement. The observations can be transferred into a task list of items that need to be implemented. At this point, it’s up to you as to how to proceed next! You can choose to make the corrections noted in the report yourself or you can enlist PCCA’s Implementation Services to perform all of the report recommendations.
Your PCCA Specialist will spend time at your facility, working with you to improve the quality of your facility and processes to ensure your compliance with USP <797> and <795>. Your Specialist will work with you to achieve your compliance goals in a cost- effective and timely manner.
PCCA assistance includes: