Professional knowledge. Practical application.

Knowledge built for real work.

Practical digital training and professional document systems for laboratory, quality and GMP teams — developed from real experience and designed for active use.

Online coursesInteractive professional learningDocument systemsEditable SOPs and templatesEvaluate us as a supplierReview IC GLOBALTEST OOD as your provider

Digital product catalogue

Learn. Apply. Improve.

Why professionals choose Q-VALISMore than information. Knowledge you can use.
Real experience

Built from work in regulated environments.

Practical application

Designed for confident everyday use.

Professional depth

No superficial content or meaningless certificates.

Lasting value

Knowledge and resources that remain useful.

Online course
EU GMP

EU GMP - Good Documentation Practice & Data Integrity

An interactive, scenario-based course on good documentation practice and data integrity in EU GMP-regulated environments. It develops the practical judgement needed to create, review, correct and protect reliable records and trustworthy data throughout their lifecycle.

Certificates compatible withEuropass — European UnionEuropean Digital Credentials for Learning
Under construction
Course preview
Document system
EU GMP · EU AI regulatory framework

AI Use in GMP Environments — Complete SOP System

A complete, editable SOP with all supporting appendices for the controlled use of AI in a GMP environment, developed with applicable EU requirements for AI, data protection, confidentiality, intellectual property, cybersecurity and data integrity in view.

Planned contents
  • Editable SOP and controlled governance workflow
  • Risk assessment, approval and authorised-use controls
  • Supporting forms, registers and practical appendices
In development
Document system
EU GMP Annex 15

Equipment Qualification in a GMP Environment — Complete Document System

A structured, editable document system for planning, executing and recording the qualification lifecycle of GMP equipment, covering DQ, IQ, OQ and PQ in line with EU GMP Annex 15.

Planned contents
  • DQ, IQ, OQ and PQ lifecycle documentation
  • Editable protocols, reports and practical checklists
  • Traceable review, approval and qualification records
In development

The Q-VALIS approach

Professional training should require attention.

Q-VALIS is designed for professionals who need knowledge they can use, not simply content they can play in the background. Every course combines structured explanations, voice-over, complete transcripts, knowledge checks and applied cases.

The learner remains actively involved throughout the course and demonstrates understanding before successful completion. Requirements, assessment rules and the exact learning outcome are stated clearly before purchase.

01

Built for application

The purpose is not simply to repeat requirements. We explain what they mean in practice and how they affect real decisions, records and responsibilities.

02

Active participation

Learners answer questions, assess situations and work through realistic cases. Progress requires attention and demonstrated understanding.

03

Developed by practitioners

Content is created and reviewed by professionals with long-standing experience in laboratories, quality systems and regulated environments.

04

Traceable completion

Course progress and assessment are documented. Successful completion leads to a uniquely numbered certificate that can be verified online.