Interpretation, application and anticipation of legislative changes are essential elements of effective compliance strategies within regulated sectors.

TT’s expertise in delivering validated/accredited cGMP facilities extends across the pharmaceutical, biotechnology and medical industries.

Our facilities & engineering services provide complete solutions wherever efficient, cost-effective compliance is required.

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TT’s validation processes cover every stage of project development, from initial concepts through to project design, construction and commissioning.

Our validation protocols and documentation management systems ensure continuous improvements and successful outcomes from inspections by the regulatory authorities.

Our support documentation is generated and verified at source, reducing the normally intensive back-end validation effort. This allows us to concentrate on more important functional testing rather than document collation, thereby reducing project timescales.

We apply true project management principles to our validation processes, combining transparent progress monitoring systems with efficient, value-for-money service.

Our philosophy of continuous improvement and our leading edge validation processes ensure effective delivery of an unparalleled range of services.

  • cGMP Audits
  • Regulatory Authority Inspection Assistance/Submission Portfolios
  • Development of User Requirement Statements
  • Validation MasterPlanning
  • Validation Protocol Development & Execution
  • Validation Progress Tracking Systems
  • PQ Assistance
  • Revalidation Programmes
  • Validation Management Systems
  • Training Programmes
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