IT Solutions / GAMP / Data Integrity (RDI)

Tarqvara Pharma Technologies offers services in the field of computer technologies and monitoring and control systems for the pharmaceutical industry, including:

1. Consulting on GMP/GAMP, 21 CFR Part 11, and Records and Data Integrity (RDI) requirements as applied to computerized systems and systems controlled by industrial controllers (PLCs).
2. Expert support for IT developers and pharmaceutical enterprises regarding the architecture, implementation, and testing/validation of PLC-based and computerized systems in compliance with regulatory requirements of the pharmaceutical industry.
3. Development and supply of proprietary GMP environmental monitoring systems (EMS) for cleanrooms and processes, such as the Tarqvara GMP Monitor, with a complete validation package in compliance with GMP / GAMP5 / 21 CFR Part 11.

The specialists at Tarqvara Pharma Technologies have extensive experience in computer technologies and monitoring and control systems for the pharmaceutical industry, in accordance with international, European, and national regulatory requirements and standards.

See also:
GMP/GxP Consulting
GMP Monitoring Systems
Tarqvara GMP Monitoring System
Computerized Systems Validation (CSV)