How CDMOs can win sponsor trust with an audit-ready QMS
When pharma companies evaluate your CDMO for a potential partnership… You want to make sure that your QMS is:
✔️Solid
✔️Transparent
✔️Audit-ready
Because it takes one failed audit to go off-rails. 😮💨
Join this webinar and learn how to stay audit-ready and gain a competitive edge with an eQMS like Scilife.
It only takes one failed audit.
And all those partnerships you’ve worked so hard to build— gone in seconds.
Because when pharma companies evaluate Contract Development and Manufacturing Organizations, one of their main considerations is how solid their QMS is.
That’s why we’re bringing you this webinar: to help CDMOs stay audit-ready and gain a competitive edge with an integrated eQMS like Scilife.
We’ll show you how to:
- Keep documentation and records organized to stay always audit-ready.
- Enable sponsor oversight with traceable data and secure access.
- Track and close CAPAs with clear ownership and audit trails.
- Centralize your QMS to eliminate silos and scattered tools.
- Strengthen your positioning by demonstrating transparency and control.
Join Jordi Ametller, Account Executive, who will be running the webinar, and Angel Buendía, Knowledge Manager, who will be moderating the session.
📅 July 24th, 2025 | 11:00H (CEST)
Find your competitive edge. Win trust and build lasting partnerships through audit readiness and smart quality.