Team Tranquil provides full range of support and assistance to industries regulated by FDA in meeting 21 CFR Part 11 compliance.
We support our customers in many areas of Computer System Verification and Validation including; Project Management, IQ/OQ/PV Protocol Preparation and Execution, SOPs, Audit Reporting, Change Control, etc.
Team Tranquil has a wide range of knowledge and experience on various areas and projects:
- Analytical Sciences:LC/GC/MS, LIMS
- Manufacturing:ERP, LIMS
- Regulatory:Electronic Submissions
- Servers and Workstations Hardware and Software, Network Infrastructure
Team Tranquil offers global services, from User Requirements Specifications to Validation Reports, to help clients improving performances and achieving compliance efficiency.