By Learning From Experts
Spanning The Pharmaceutical Industry
Understand Cleanroom Requirements, Proposed USP Changes, Insanitary Conditions, & More
Industry Thought Leaders & Influencers Present Topics That Offer Exceptional Benefit To You
Protect yourelf, patients, and environment from exposure to hazardous drugs.
Mitigate risk by allowing Eagle to verify that sampled areas were appropriately cleaned.
October 26th, 2022
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
EAGLE SEMINAR 10/26 | Learn from industry experts at this in-person event.
Attendees will gain an understanding of cleanroom requirements, environmental monitoring, proposed changes to USP, insanitary conditions, stability studies, and transitioning from 503A to 503B.
Compounders on Capital Hill was a home run!
Thank you, Alliance for Pharmacy Compounding (formerly IACP), for the ultimate event! It was a pleasure meeting people who make a positive difference for pharmacy compounding and their patients. View Us On LinkedIn.
EAGLE had a great time @ the 2022 PDA/FDA Joint Regulatory Conference
A great time was had at the #PDA/FDA Conference! Thank you to everyone that came by to visit David Hussong, Ph.D., Ross A. Caputo, Ph.D., Lisa Johnson, Jacqueline Esqueda, PharmD, Ashley Trueheart, and Miguel Hernandez Alonzo. We really enjoyed the conference and are looking forward to seeing you all again soon. View Us On LinkedIn.
🏜️ ashp's Summer Meeting & Exhibition was great!
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.