Globiox can conduct Good Laboratory Practices (GLP) audits of client laboratories to ensure compliance with FDA (21 CFR 58, EMA (2004/10/EC), and other country’s regulations. GLPs are critical for generating data suitable for supporting drug and medical device development, approval, and commercial sale.
Globiox's team of expert GLP auditors ensure your company has conformed to ever changing relations. Below is an abbreviated list of some GLP audits we perform. If you require a specialty audit, or an audit type not listed below, contact our team for a free evaluation of your needs.
- Sponsor and Contract Laboratory Audit
- GLP Laboratory Design Audit
- GLP Validation Audit
- Supplier Audit
- Data Integrity Audit
- Mock FDA and EMEA
- Quality Systems Assessment
- Utility Design
- Management Strategy Evaluations for Quality Assurance and Quality Control Systems