SaaS goes GxP –
How to make your software fit for the regulated life sciences market
Entering the pharma, biotech or medical technology market requires SaaS vendors to have a clear understanding of regulatory requirements – and the ability to meet them safely and confidently.
In this webinar, we show you how to systematically prepare your software and organization for the GxP-regulated market – efficiently, transparently and without unnecessary bureaucracy.
Webinar Content
- GxP basics (GMP, GLP, GCP) – clearly and understandably explained
- Role and responsibility of SaaS vendors in the regulated environment
- Requirements for QMS, software development and change and release management validation of cloud and SaaS solutions from the customer perspective
- Typical audit requirements – and how to prepare for them
- A proven step-by-step approach for structured market entry
Dates
Friday, May 29, 2026, 10:00 – 10:45 AM (webinar in English)
Can’t make these dates? Register anyway to secure access to the free podcast! You will receive the access details automatically shortly after the web session.
Target Audience
This webinar is aimed at:
- SaaS and software vendors with little or no GxP experience
- Cloud providers with inquiries from the life sciences industry
- CEOs, CTOs, product owners and quality and compliance managers
- Companies with strategic growth targets in regulated industries
Your Benefits
After the webinar, you will know:
- Which regulatory requirements are truly relevant for your company
- How to build GxP readiness in a structured manner
- How to win trust with regulated customers
- How compliance can become a competitive advantage
Participation and Registration
Our webinars are a free service for customers and prospects of DHC.
IT service providers and consultants are excluded from participation.
The number of participants is limited.