PRISYM ID is dedicated to ensuring that we exceed your expectations when implementing our world-class labeling solutions.

Our experienced professional services team can add value and reduce cost at all touch-points of your label production process including URS support/build, project management, validation, health-checks, training and support & maintenance.

PRISYM ID recognizes the importance of delivering support services with not only the requisite technical knowledge but also with the understanding of your regulated markets. No other company has the same understanding of label lifecycle management or the unique constraints of the life sciences arena.

Our team of in-house compliance and validation subject matter experts, with many years’ experience of working with life science organizations, are available to support on project planning, risk assessment and testing implementations, as well as supplying scripts and full documentation to support the validation process.

Professional services and support teams based in Boston and the UK comprise of experts with extensive, first-hand experience of the delivery and support of successful label and artwork projects across the highly regulated life science sectors; with members of the team having worked on more validated solutions than all of our competitors put together.

Services Datasheet 1 - PRISYM ID Client Support Services PRISYM ID Client Support Services Posted in: Data Sheet -

PRISYM ID is dedicated to ensuring that we exceed your expectations when implementing our world-class labeling solutions.

Our experienced professional services team can add value and reduce cost...

Read More


With sites in Europe and the United States, PRISYM ID delivers outstanding 24/7 global support. We reduce the associated risks and overheads that a CAT 1 interruption to production can cause, offering highest priority response and resolution. Our in-house support team of experienced and dedicated engineers commit to dealing with your query within a fixed time frame, ensuring minimum disruption, critical to any labeling process.

Our software is supplied as a validatable package, including auditable security protocols, IQ/OQ scripts and lifecycle documentation, based on the GAMP 5 Model.

Installation Qualification (IQ) – during deployment, our experienced Implementation Consultants are available to perform or oversee the installation and configuration of your system. This provides a more rapid deployment of systems while minimizing risk to your project delivery timeline.

Operational/Performance Qualifications (OQ/PQ) – Our Implementation Consultants complete our OQ and assist many of our clients with the PQ test and validate of their solution against a wide range of technical and operational challenges and requirements, improving quality and efficiency in both the testing process itself and the delivery timeline.

We offer on-site consulting as well as execution of operational tasks to get you into production quickly with new and/or existing products. Examples of tasks offered are:

  • Label format design
  • Label consolidation
  • Data import
  • Custom configurations
  • Printer setup
  • Historic reprint.

Our project managers are here to add value at every step of your implementation including planning, organizing, motivating, and controlling resources to achieve your organizations specific goals.

We offer training courses which will strengthen the skills of your users in several areas of your label lifecycle management solution including:

  • System Admin & Support
  • Label Design
  • Workflow & Approval.
  • We can also tailor a training program to suit your individual requirements, and delivered at your facility.

Our Advisory Services include:

  • An onsite engagement to evaluate the complete global label lifecycle process from design, workflow, and production processes (URS)
  • An evaluation of the current label print processes, including reconciliation, reprint, and relabeling
  • Regulatory compliance guidance, specifically FDA 21 CFR Part 11, UDI and EU MDR
  • GAP analysis to identify the functional area(s) that would provide the greatest return on investment
  • Risk review and best practice summary, including standardization, data management, workflow processes and process control