CIP and SIP System

CIP and SIP System
Product Description

Pharmatech offers CIP/SIP combo complete system, Self contained portable system that is easily programmed to accommodate in wide variety of single use, recirculated CIP applications. It is designed for highly critical cleaning solution, while meeting cGMP & ASME-BPE standards. Combined with Unique SIP system followed after CIP cleaning, designed to provide documented temperature controlled sterilization cycles in accordance with desired procedure using pure steam. The recipe is user definable & generates a validated output. Fully automated system functions involving integration of sanitary automatic valves & requisite instruments enabling control & monitoring of critical parameters throughout the complete cycle. It is provided with Interface Screens, Multilevel Passwords & Fault Message displays. DQ/IQ/OQ qualification documents & validation support are provided.

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Pharmatech Process Equipments

  • IN
  • 2015
    On CPHI since
View company profile
Categories
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Specifications
  • CAS Registry Number
    0000-00-2
  • Supplied from
    India
More specifications Fewer specifications
Sales Markets
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Pharmatech Process Equipments

  • IN
  • 2015
    On CPHI since
View company profile

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Pharmatech Process Equipments resources (1)

  • General E-Catalogue - Pharmatech Process Equipments

    Brochure General E-Catalogue - Pharmatech Process Equipments

    Pharmatech Process Equipments is subsidiary of Pharmalab India Pvt. Ltd. The company has significantly contributed towards the growth of the pharmaceutical Industry by Investing in Innovative technology and equipment designed to augment efficiencies and profitability. Pharmatech offers turnkey solutions for Liquid Processing Plants comprising of Inter-Connecting piping and automation systems. These comprehensive solutions find application in Pharmaceutical, Biotech and Cosmetic Industries. Pharmatech offers the consultation of conceptualized design, detail engineering , manufacturing, testing , supply, Installation and validation of the processing system as per URS and in strict compliance with cGMP, USFDA, ASME (BPE), "CE" & EHEDG guidelines.