Validation & Qualification of Equipment and Processes (Validation & Qualification)
- Design of Equipment and Facilities Validation Program
- Writing and Execution of IQ/OQ/PQ
- Process Validation, Computerized Systems Validation (CSV), Cleaning Validation
(Validation & Qualification)
DQ, IQ, OQ Documents
Providing IQ, OQ, PQ Services for Critical Equipment and Machinery
Process Validation
Design and Implementation of Validation Programs for Process, Manufacturing, Production, and Control
Computerized Systems Validation (CSV)
Validation of Software and Automated Systems Based on GAMP 5
Cleaning Validation
Sampling Planning and Data Analysis for Validation of Equipment Cleaning Effectiveness
Preparation of Documentation and Protocol
Preparation of formal documentation such as URS, protocols, and related documents
Why AVISAN?
Specialized Experience in Sensitive Industries
Validation teams familiar with GMP
Flexible approach and global regulatory mindset
