Industries Life Sciences Join us for a webinar on ValidAId

Webinar ValidAId: Supercharge your validation process with AI

See how to create URS, test protocols and summaries in minutes. Spend less time searching and more time validating with full traceability and compliance.

PRACTICAL DETAILS:

  • September 16th | 10:30 – 12:00
  • Microsoft Teams

SUPERCHARGE YOUR VALIDATION PROCESS

Register your place in the webinar

Create quality documents fast

Generate URS and test protocols in minutes with validation specific workflows and styles.

Find what matters

RAG pulls from validated sources like manuals, SOPs, work instructions and IQ/OQ/PQ templates.

Stay compliant

Every answer has traceable sources so reviews and audits run smoother.

Knowledge base

We load device and software manuals, SOPs, work instructions, and IQ/OQ/PQ templates into a searchable knowledge base so ValidAId can retrieve and generate precise outputs.

Testing protocol

ValidAId compiles protocols with traceability. You verify tests quickly and adjust details without regenerating the full document.

User interactions

Use an MS Word assistant for paper based workflows or a web plugin and overlay UI for paperless validation so teams can work the way they prefer.

 

WHY ATTEND

What you’ll learn

  • How ValidAId speeds up your validation workflow
  • Live demo of URS and protocol generation
  • Best practices for safe use in GxP contexts
  • Q&A with our experts

 

Register

Who should attend

  • Validation consultants and engineers
  • QA and CSV teams
  • Team leads who want less documentation pressure
  • Anyone with a genuine interest in AI & Validation

 

Register

Register today & discover the benefits

  • Up to 30% faster for documentation thanks to targeted AI support.
  • 75% of users more productive in daily validation work.
  • RAG over manuals, SOPs, work instructions, and IQ/OQ/PQ templates.
  • Traceability and compliance in every step.

Why ValidAId beats generic AI tools

ValidAId

✔ Purpose-built for validation in regulated pharma environments
✔ Uses only validated sources and industry-specific language
✔ Predefined workflows for accuracy and consistency
✔ Traceable, auditable output every time

Generic AI

✘ Broad, non-specific knowledge
✘ No guarantee of source accuracy
✘ Needs heavy prompting to get usable results
✘ Not designed for compliance