Resources & Inspiration
Upgrade of Kneat SAAS Platform – Why It Matters and How to Succeed
The pharmaceutical industry is under constant pressure to deliver safe, compliant products while accelerating time-to-market. Traditional paper-based validation processes are time-consuming, error-prone, and difficult to
Outsourcing of GMP Audits: Practical and Regulatory Aspects
Conversations That Matter No deviation’s Takeaways from ISPE France Conference – Outsourcing and Supplier Management in the Pharmaceutical Industry Speaker: Jean-Denis Mallet – Former Inspector, Auditor,
Rouge and Elastomer Management in Biopharma
Rouge and Elastomer Management in Biopharma: Hidden Risks, Smarter Strategies The foundation of biopharmaceutical operations lies in process accuracy, system robustness, and regulatory adherence.Yet two
Kneat in Action: Beyond Traditional CQV Boundaries
Validation in the pharmaceutical industry is evolving fast — and Kneat is right at the heart of this transformation. Far beyond traditional Commissioning, Qualification, and
GMP-Compliant Maintenance: A Pillar of Process Control
GMP-Compliant Maintenance: A Pillar of Process Control In Good Manufacturing Practice (GMP), the third phase of process validation—continued process verification—ensures that your process remains in a state
Mobilizing a Digital Engineering Program: Practitioner View
Conversations That Matters No deviation’s Takeaways from ISPE Facilities of the Future Conference in San Fransisco Mobilizing a Digital Engineering Program: Practitioner View Speaker: Joydeep
No deviation joins Fedegari
We are excited to share news of great significance to our journey: No deviation officially joins the Fedegari Group. This union represents a unique opportunity
Remote Audits – Are You Ready?
Auditors show they are ready for remote audits, are you? The pharmaceutical industry is undergoing a transformation in regulatory oversight, driven by the increasing adoption
