BRIEF INTRODUCTION

Cleaning, Sterilizing and Drying in Place of Pharmaceutical, Biotechnology and Cosmetic equipment is the most appropriate and safe method for managing these critical and frequent operations

Our wide experience in engineering and manufacturing equipment and complex systems for liquid, semisolid and solid products has allowed us to design and manufacture the most appropriate and fully performing automated CIP/SIP/Drying units perfectly executing the different applications

TECHNICAL DESCRIPTION

CIP/SIP units are provided with one or two purified water buffer tanks, sanitary heat exchanger to heat up the washing solutions, detergent/chemical dosing groups in order to optimize the cleaning in place and conductivity meters, pH and TOC instruments to analyze the quality of washing solutions

OUR DESIGN CONSIDERS:

• Sophisticated control systems for automatic/semi-automatic operations/receipts in compliance with 21 CFR part 11, controlled by PLC and SCADA
• System design BPE/ASME, fully compliant with EU cGMP and FDA requirements
• Minimized water consumption during CIP cycles thanks to an optimized process design