Learning and Resources for Regulated Industries
Professional training, implementation systems and practical resources for people working in regulated industries.
Q-VALIS products
Practical, scenario-based training in EU GMP Good Documentation Practice and Data Integrity. Work through structured modules, knowledge checks and practical cases at your own pace. Successful completion of the learning activities and Final Assessment leads to a verifiable Certificate of Completion.
9 modules · Self-paced · English
12 months from individual activation
Version 1.1
Version Date: 15 October 2026
Ph. Eur. 2.6.12 & 2.6.13
Professional online reference for pharmaceutical QC microbiologists covering practical method suitability under Ph. Eur. 2.6.12 and 2.6.13.
Read anytime in your Q-VALIS account.
Includes editable Method Suitability Report Template (.docx)
Online Technical Guide · English
Version 1.0
Version Date: 9 October 2026
Editable SOPs, supporting document packs and digital tools for controlled AI use in a GMP environment.
Document packs + Digital tools
Documentation, digital tools and dedicated training for the DQ, IQ, OQ and PQ qualification lifecycle.
Document packs + Digital tools
The Q-VALIS approach
Q-VALIS provides structured training, implementation systems and practical resources designed for regulated environments. Each product is built around clear objectives, defined content and practical application — not passive viewing alone.
Where applicable, individual progress, assessments and completion are recorded, and uniquely numbered Certificates of Achievement can be verified online.
Provider qualification information