ICSVC takes to heart its mission, to support the continued growth and development of the Pharmaceutical, Biotechnology and Medical Devices industries by facilitating collaboration and communication among key stakeholders. To that purpose, different partnerships are put forwards, not only during this ICSVC first edition, but before and between editions!
As pharmaceutical, biotechnological and medical devices industries faced CSV innovations but at different stages, these partnerships are adapted according to the specificities and needs of each.
Validfor is a next-generation, AI-enabled Validation Lifecycle Management (VLM) platform purpose-built for regulated pharmaceutical, biotech, medtech, CRO, and CDMO environments. Their technology reshapes the way teams create, manage, trace, and maintain validation documentation; bringing intelligence, structure, and automation to every stage of the lifecycle.
What we deliver:
🖥Data-driven Validation: a modern approach that transforms validation from document-heavy process into structured, interoperable, and intelligent data flows.
⚙️AI-Enabled Guidance: our embedded AI consultant provides expert-level support, helping teams make faster, smarter, and compliant decisions.
💯 Full lifecycle Digitalization: from requirements and risk assessments to design, testing, traceability, and periodic reviews. All stramlined in a single platform.
✅Compliance by Design: pre-configured with industry best practices and regulatory expectetions while fully adaptable to each organization's needs.
📃Audit-Ready Confidence: time-stamped records, automated traceability, and complete transparency provide a solid foundation for regulatory inspections.
But beyond the technology, Validfor shares something essential with ICSVC:
👉 a belief that the future of validation must be digital, connected, and continuously improving
