
USP <797> <800> Sterile Compounding | Identifying Resources to Support Your Compliance Efforts
Identifying and Prioritizing Needs USP <797> USP <800> What to do Once a QA Program is in Place Keys to Choosing a Vendor Key Questions

Identifying and Prioritizing Needs USP <797> USP <800> What to do Once a QA Program is in Place Keys to Choosing a Vendor Key Questions

What to do When Building/Renovating Your Pharmacy Assemble the Team: Common Mistakes Resources: Design: Construction: Post-Construction: Q

An Environmental Sampling Plan Confirms the Effectiveness of: Typical Environmental Tests *<797> Revision requires continuous monitoring devices Keys to a Successful Sampling Plan Common Challenges

Testing and monitoring of your Cleanroom, HEPA filters, and Biological Safety Cabinets/Laminar Flow Hoods/Clean Benches/Fume Hoods must occur on a routine basis to guarantee personnel

Why USP<797>? Why USP<800>? USP <797> <800> November 2023 Management Strategies Quality Assurance Program How Quality Solutions Can Help EM Kits Ensuring a Return on

As of November 2023, a third revision of USP<797> became official along with USP<800>. Sterile Compounding Pharmacies around the country, in conjunction with State Boards

Quality Solutions can assist in establishing requirements for your pharmacy operations while identifying appropriate facility solutions. Our vast experience with new and retrofitted facilities allow

Introduction / Vision Started in 2001 as a validation and regulatory services provider, Quality Solutions is continually developing a portfolio of services to provide a
Tailored facility servicesCost-effective, in-house alternativeCustom evaluation and risk assessment
As the demand for personalized medications grows, so does the scrutiny on compounding pharmacies. Here are the top 5 compliance issues that could impact your