Pharmaceutical Systems Validation

Pharmaceutical Validation Services Available Nationwide

Our team of practiced experts has experience identifying areas for improvement in various strands of a variety of pharmaceutical companies. Our solutions are comprehensive and all-encompassing, covering Pharmacogenomics, Pharmacovigilance, Bio Informatics and laboratory informatics (LIMS) requirements.

This end-to-end service ensures the effective running of industry development and ensures compliance with Federal and European regulations.

Our pharmaceutical validation services around the UK enable companies to excel in productivity, efficacy and profit.

A complete list of our services is as follows:

Pharmaceutical Validation Services Available Nationwide

The validation of your computer systems is an ongoing process that requires regular re-evaluation. It should be considered as an integral part of any computer system’s life cycle. Our pharmaceutical validation services come into play either once you’ve identified the need for a new computer system or when you’ve identified the need to bring an existing system into a qualified state. Technology develops quickly and systems that may have been state-of-the-art upon their inception can quickly find themselves out of date. Our team will help you evaluate legacy systems, automate processes, where relevant, and adhere to regulations, with comprehensive project planning and oversight available throughout.

This Service Includes :-

  • 21 CFR Part 11 Compliance
  • Software Quality Assurance
  • Software Testing
  • System Support and Training
  • Audits and Assessments

Process Validation

Our service for process validation ensures that the processes set in place by your company consistently produce the desired outcomes – rendering products that meet requirements on quality and specification. This could include the analysis of manufacturing, packaging and sterilisation processes within the pharmaceutical industry.

Our validation services can be broken down into three sections:


Process Design :-

Our team will work with you to develop an understanding of the desired outcomes of the process in question, before developing said process, along with a strategy to ensure process control throughout.

Process Qualification :-

The process we have designed will then undergo thorough evaluation to ensure that the required outcomes are being met. We will also evaluate the ongoing reliability of the process as it pertains to efficient commercial manufacturing. We’ll repair a final report and take measures to ameliorate any imperfect elements.

Continued Process Verification :-

As routine production is carried out, ongoing verification will be performed, to ensure that the process is stable. We will undertake periodic assessments of the process also, to identify and undertake necessary alterations or recalibration of the process.

Cleaning Validation

Thanks to the expertise of our experienced staff, we can construct and execute master plans for cleaning development and cleaning validation. We begin with a hazard identification process and examine cleaning processes in-depth, to ensure that all potential hazards are identified and mitigated before they have the chance to exacerbate. This includes chemical and microbiological hazards, as well as API, cleaning agents and Micro/Endotoxins usage in your workplace.

Pharmaceutical Validation Services Available Nationwide

Validation Network offer pharmaceutical validation services, ensuring that all utility and HVAC systems are qualified and in pristine working order. We will inspect your system thoroughly before qualifying it if it meets the required specifications. We can qualify brand-new systems, as well as issuing change control documents for the modification of existing systems. Our services are available on an independent basis or, alternatively, we are able to work with system vendors in the generation of specific relevant test documents and scripts.

Types of utilities that we validate include :-

  • Gas Systems (CO2, Nitrogen)
  • Electrical
  • Waste Disposal
  • HVAC Building Automation Systems
  • Steam Generation
  • Compressed Air
  • Storage Tank Systems
  • RO (Reverse Osmosis)
  • UF (Ultra Filtration)
  • PUR (Purified Water)
  • WFI (Water for Injection) Hot or Variable Temp
  • Loop Distribution Controls
  • Distillation Systems

Pharmaceutical Validation Services Available Nationwide

By law, any and all equipment used in the storage, production, packaging or quality control testing of any cGMP product must submit to proper validation. This includes all electronic, mechanical or automatic equipment, which must be checked, inspected and, if necessary, recalibrated on a routine basis. This must be done in accordance with a specific written program, designed to ensure effective performance.

Our expert team are adept at providing validation services and specialise in the following types of equipment:

Analytical Lab Equipment :
  • Spectrophotometers (UV/VIS, IR, FTIR)
  • Protein Sequencers, Flow Cytometers, Micro Readers, Plate Readers
  • Refrigerators, Freezers, Ovens, Incubators, Autoclaves
  • MB Laminar Flow, Biosafety Cabinets
  • Titrators, Dissolution, Stability Chambers
  • Degassers, TOC Analyzers, dPCR and ddPCR
Software and DAS Systems :
  • OpenLAB
  • Millennium
  • MassHunter
  • Empower
  • Chemstation
  • Chemstore
  • SoftMax Pro
  • DSC

Manufacturing Equipment :

  • Mixers, Dryers, Fluid Bed Dryers
  • Tablet Presses, Sterilization Tunnels, Tanks and Vessels.
  • Ampoule, Capsule, Syrup and Vial Fillers
  • Cartooning, Coating and Labelling
  • Cream and Ointment Filling
  • Centrifuges and Bioreactors
  • Chromatography
  • Freeze Dryer

Sterilization :

  • Dry Heat and Steam Sterilisers
  • Terminal Sterilisers
  • Isolators
  • Gas Cycle Development
  • Hydrogen Peroxide
  • Gamma Radiation
  • Steam or Sterilize in Place (SIP) or Clean in Place

Vision and Labelling Systems :

  • Labelers
  • Laser and Engraved Printing
  • Automated Vision Systems
  • Labelling and Inspection for HIBC and Barcodes

Packaging :

  • Blister Packs
  • Sealers and UDI Labelers
  • Trayers, Checkweigher Machines, Cartoners, Case Formers and Tapers, Inkjets
  • Inventory Recognition Systems (RFID)

Test Equipment :

  • Dissolution Samplers
  • Friability Testers
  • Refractometers
  • Powder Handling Equipment

Pharmaceutical Validation Services Available Nationwide

This dual service provides a comprehensive solution to your process design, implementation and streamlining issues. The commissioning side allows our experienced team to assess the necessary requirements for a specific process, as well the equipment required to effectively put it into practice. Conversely, the qualification aspect of this service allows us to assess whether the process you have constructed is ready and appropriate for its intended use. Our pharmaceutical validation services  across the UK allow us to marry these two services to ensure the best outcomes for your business processes.

Comprehensive Service Founded on Experience

For sound advice that ensures the efficient operation of your pharmaceutical systems, contact the industry experts today.


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