Commissioning and Validation (CQV)

The Validation Solutions Group is cGMP trained and well versed in all FDA validation concepts and definitions. The team offers assistance to our clients in a wide range of validations, processes, utilities, facilities, equipment, laboratory, medical devices, and computerized systems. Our commissioning and validation personnel work very closely with all groups in a combined effort to achieve a quality support program for our clients.

All personnel are trained in the planning, development and execution of commissioning and validation programs. The group consists of project managers, commissioning and validation engineers/specialists, and automation engineers/specialists.

 

Our commissioning and validation (CQV) group has access to a wealth of forms and protocol templates to support our clients for all phases in the validation life cycle. Our commissioning and validation personnel are trained in the use of current technology software tools and in the utilization of our vast knowledge-base to meet our client's needs.

 

Sample Equipment/Automation/Commissioning and Validation (CQV) Experience:

  • HVAC
  • WFI
  • USP Water
  • RO Systems
  • DI Systems
  • CIP/SIP Systems
  • Compressed Air
  • Clean Steam
  • Nitrogen/oxygen
  • Single Use Bioreactors
  • SU Bioreactor Bag Hoist
  • Harvest Vessels
  • Media Bag Agitation System
  • Robotics
  • Dry Heat Ovens
  • Tablet Counter/Dispenser
  • Cappers
  • Induction Cap Sealer
  • Syringe Filler
  • Vial Filler
  • RABS
  • Labelers
  • Vision Systems
  • Serialization
  • Pkg. Equipment Aseptic Processing
  • Autoclaves
  • Lyophilizer
  • Incubators
  • Media Prep
  • Fermentors
  • Extruders
  • Chromatography Systems
  • Lab Equipment
  • Torque Meters
  • Fluid Bed Granulation /Drying
  • Wet & Dry Mills
  • Tablet Compression
  • Coaters
  • Gel Dippers
  • Printers

 

 

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AUTOMATION & VALIDATION SOLUTIONS, INC.

725 Skippack Pike, Ste. 380

Blue Bell, PA 19422

(215) 542-7917

info@avs3.com