Revisions to the USP compounding chapters
and were published and will be official on November 1, 2023. These revisions will make USP compendially applicable.
Eagle offers multiple products and services to stay compliant with the revisions.
USP ENCOURAGES EARLY IMPLEMENTATION.
Get ready with Eagle!
Utilize our industry experts to ensure that you are in regulatory compliance with the revisions. With our guidance, you will feel confident with your compliance. Let our experience work for you.
Protect yourelf, patients, and environment from exposure to hazardous drugs.
Mitigate risk by allowing Eagle to verify that sampled areas were appropriately cleaned.
✓ Fast Results
✓ Easy to Use
Your fast and convenient method for verifying the efficacy of your cleaning program.
Let our experts conduct a Gap Analysis Audit of your facility to determine compliance with regulations and standards. Our audit will identify areas where your operation needs improvement in order to achieve compliance. Take the guesswork out of compliance. Be prepared for regulatory inspections.
Our scientific experts excel at helping sterile and non-sterile facilities identify challenges, risks, opportunities, and implement cost-effective, science-based solutions. With our guidance, you’ll feel confident with your compliance.
With our highly qualified interdisciplinary team, Eagle is uniquely positioned to accommodate your distinct needs, with services in consulting, calibration, certification, facility design, quality systems, third-party audits, and more.
The Chemistry Department offers a wide range of testing options in accordance with regulatory requirements, including CGMP, USP, and DEA. Ensuring high-quality results, accuracy, and customer satisfaction is our top priority.
The Microbiology Department provides customers with compendial testing that supports product disposition, development, validation and compliance with regulatory guidelines and requirements.
Our engineers can provide initial and ongoing ISO certification of your facility to support aseptic operations. As well as qualify and calibrate your equipment to assure proper operation and performance.
Showcasing Eagle’s Talented People and Events
Meet EAGLE @ ASHP Midyear! | Las Vegas | 12/04-07
Join EAGLE, pharmacy professionals, & students from all over the world at #ASHP22. Meet EAGLE’s President & CEO Ross A. Caputo, PhD., VP of Marketing & Business Development Lisa Johnson, BS, & Senior Business Development Specialist Jacqueline Esqueda, PharmD, Rph. Their experiences span the healthcare and pharmaceutical industry with expertise in USP 795, 797, 800, and CGMP. Click for details.
EAGLE celebrates Jacqueline Esqueda, PharmD!
USP Announcement 🔺
The long-awaited revisions to USP compounding chapters <795> & <797> were released & will become official on Nov 1, 2023. USP ENCOURAGES early implementation.
EAGLE is here for you to answer the questions & guide you through the implementation process.
EAGLE Pre-Seminar & PCCA International Seminar was amazing. | #ISX22
Thank you to PCCA for putting on a great event & thank you to all those who attended. From online to in-person, everyone was engaged, learning occurred and connections were made. We look forward to seeing everyone at future events. May the rest of your 2022 be great & your 2023 be greater! IMAGES FROM SEMINAR.
Highlighting Eagle’s Expertise
What It Means When Your Sample is Out-Of-Specification
When sending samples for testing at third-party facilities, most clients want to ensure that results are both accurate and provided in a timely manner. This article intends to summarize the OOS process.
Leveraging Our Expertise On Your Behalf
Regulatory requirements from the FDA, State Boards of Pharmacy, DEA, and other regulatory authorities can be difficult to understand, interpret, and implement. That is why, in addition to science-based testing and statistical analysis, Eagle offers consulting services and third-party (gap analysis) audits in accordance with your distinct regulatory needs. Let us help you meet your unique needs as a pharmacy, 503B, or CGMP manufacturer.
The World’s Fastest FDA-Accepted Sterility Test
SCANRDI® has revolutionized the rapid microbial detection of organisms in solutions and soluble products with speed and sensitivity that is unrivaled. Eagle’s SCANRDI® Sterility Test Protocol is an FDA-accepted alternative to the official USP <71> sterility test that can take 14-18 days to complete. Let Eagle, an industry leader in SCANRDI®sterility testing, deliver your test results in as little as 1 business day.