US Validation Services, Inc. provides FDA-regulated industries such as the
Pharmaceutical, Biotechnology, and Medical Device, with validation services
which will satisfy the stringent demands of current Good Manufacturing Practice
(cGMP) Regulations and Quality Systems Regulations (QSR).
We can support your efforts allowing you to complete your project on-time and
on-budget, while assuring compliance with the current industry regulations and
standards.
Electronic Log Book (eLogBook) application, developed by U.S. Validation Services in affiliation with
Control Quest, Inc. allows users to maintain equipment and software
modifications while addressing compliance capabilities. Users can record, manage
and track changes in records associated with processes, equipment and software.
Our eLogBook provides both Event Logs and Data Logs. Event Logs trace changes in
software, equipment alterations and other more general events, whereas Data Logs
track specific process parameters.
Validation Services We Offer
- Equipment Validation
- Utility systems Validation
- Facility Qualification
- CFR 21, Part 11 Electronic Signatures, Electronic Records Consulting
- Validation Master Plan Development
- Validation Program and Project Management
- Calibration Program Auditing, Development and Optimization
- Computerized Systems and Software Qualification
For Details visit our Validation Services page.
