The Antech GLP Difference
Ensuring the quality of data — its consistency, reproducibility and reliability — is at the heart of everything we do at Antech GLP. Our system is designed to meet the most stringent GLP regulations, including our own on-site Quality Assurance team who provide oversight of all GLP studies conducted at Antech GLP.
Antech GLP is fully compliant with the GLP (Good Laboratory Practice) Regulations, as set forth in 21 CFR Part 58, as well as other regulatory requirements. We have successfully passed audits by the FDA and welcome all our clients to come see our laboratory for themselves.
On-site Quality Assurance
Our expert, on-site Quality Assurance team plays a critical role in ensuring the absolute integrity of the clinical trial process, with fully regulated documentation to ensure results can be submitted for toxicology studies, safety efficacy studies, animal health clinical trials, medical device studies, and any other studies requiring FDA approval.
Reporting and Archiving
Draft reports delivered via pdf or Microsoft Excel within 24-48 hours from receipt of samples for routine tests. For GLP studies, QA audited data reports are typically delivered within 2-3 weeks upon receipt of final samples. Raw data can be archived per 21 CFR Part 58 or returned. An electronic copy of raw data is maintained at Antech GLP for returned studies.
We make it easy to find everything you need, along with protocol assistance, sample collection, and other ways we can empower your research.
