CTP SYSTEM, with the ENGINEERING&VALIDATION Department, supports its customers to manage and directly perform all tha validation phases.
CTP has extensive experience in the preparation of Validation Master Plans at all levels, whether for an establishment or for single project, on behalf of the main international companies for all types of pharmaceutical products (APIs, solid and liquid forms, sterile products and more).
CTP performs the validation for all the automation systems, from a single equipment control system of a single machine to complex Distributed Control Systems (DCS) and Building Management Systems (BMS).
CTP Team is composed of Engineers, Chemists, Pharmaceutical experts and Biologists who, through the skills of qualified Technicians, manage and perform Qualification activities for all kinds of equipment and systems in the Pharmaceutical and related Industries. Moreover, CTP has consolidated expertise in helping clients to solve the problems that frequently arise for documentation deficiencies and other technical aspects.
CTP SYSTEM services:
- GAP Analysis
- Risk Analysis / Impact Assessment
- Design Qualification
- Validation Master Plan Preparation
- IQ / OQ / PQ of Manufacturing Equipment & Critical System
- Analytical Equipment Qualification
- Maintenance & Calibration
- Metrology Plan
- Preventive Maintenance Plan
- Specialised services (vacuum, thermography...)
For technical information:
Mob. +39 (348) 2413558