Healthcare manufacturers are well aware of the importance of microbiological testing to ensure their product’s safety and efficacy. The constant threat of product or plant contamination requires ongoing vigilance.
At AAIPharma Services, we provide you with 30 years of microbiological expertise developed from serving the biotech, pharmaceutical and medical device industries. We not only perform this testing for our customers, but as a contract manufacturer, we perform the testing ourselves on non-sterile and sterile products we make for our customers. This truly differentiates us from those who only test on behalf of third parties. This also keeps us on the leading edge of global compliance standards as we constantly upgrade our capabilities to meet the increasing needs of our global customer base.
The strictest attention to every detail ensures the performance of the methods used to test and/or monitor the conditions of your GMP manufacturing environment and the quality of products produced. Our capabilities enable you to free up resources to focus on internal programs as we become an extension of your organization. We offer a wide range of compendial and non-compendial testing services. Our core strengths include disinfectant qualification, antibiotic assays, non-sterile product evaluation (microbial limits testing) and sterile product testing including sterility testing using barrier isolation technology.
We offer:
- Technical Definition and Protocol Generation
- Method Development and Method Validation
- Testing of Formulations, Active Pharmaceutical Ingredients (APIs) and Excipients; Finished Products;
- In-process and Stability Samples
- Flexible Service Arrangements Customized to Your Business Needs
- Support for New Products from Concept to Filing
- Consulting Services to Guide Testing Needs Based on Relevant Regulations
- Troubleshooting of Product or In-plant Contamination Problems
