We're Heading to Milan – And We'd Love to Meet You
CPHI is where the pharmaceutical industry comes together, and we're excited to be part of it once again. From 6-8 October, you'll find Mavim and Cegeka together at our shared booth in Milan. Whether you're working on compliance initiatives, process improvements, or larger transformation programs, we'd love to connect and exchange ideas.
We'll be sharing how pharmaceutical organizations are creating more transparency across their operations, improving governance, supporting GMP and compliance initiatives, and helping transformation programs move from strategy to execution.
Process Governance
Create clarity around processes, ownership, systems and responsibilities.
GMP & Compliance
Support compliance initiatives and improve audit readiness.
Operational Excellence
Gain insight into processes and identify opportunities for improvement.
Digital Transformation
Connect strategy, processes and technology to drive lasting change.
Mavim & Cegeka
One Booth. Combined Expertise.
Successful transformation requires both business insight and technology expertise.
That's why Mavim and Cegeka are joining forces at CPHI Milan. Together, we help pharmaceutical organizations connect processes, technology, governance, and execution - creating the visibility and alignment needed to drive meaningful change.
Meet the Team
Schedule a meeting and we'll be happy to reserve time for a conversation.
Albert Schöberl Alessio Trussardi Dominique de Vos Gemma Gilardi Gina Zhang Henrik Walther Madsen
Cegeka Cegeka Cegeka Cegeka Mavim Cegeka
Joey Koch Joshua Schütt Matthias König Niels Wartenbergh Ola Nilsson Renata Antoniuk
Mavim Cegeka Cegeka Mavim Cegeka Mavim
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Thomas van Dorp
Cegeka
Accelerating Digital Maturity in Pharma with Cegeka & Mavim
Mavim and Cegeka combine industry-leading software and deep implementation expertise to help life sciences organizations transition into a Connected Pharma Company. By bridging the gap between business strategy and technological execution, this partnership enables organizations to navigate complex digital landscapes with total control.
By leveraging Cegeka’s customized industry blueprints built on the Microsoft Business Process Catalog inside Mavim, complex Dynamics 365 ERP and CRM implementations are heavily streamlined. This process-centric approach accelerates software delivery, secures strict regulatory compliance, minimizes implementation risks, and ensures long-term operational resilience.
Why Pharma Leaders Choose Cegeka & Mavim:
✓ Guaranteed Regulatory Compliance
Consolidate workflows to easily keep track of strict industry guardrails, validations, and documentation requirements.
✓ Enterprise Control Model
Visualize end-to-end business processes during discovery workshops before complex system configuration even begins.
✓ AI & Agent Readiness
Prepare your operational and process data to safely leverage Microsoft Copilot and automated AI agents within your ERP ecosystem.
Frequently Asked Questions
Everything you need to know about Mavim & Cegeka at CPHI Milan 2026.
Where can I find Mavim and Cegeka at CPHI Milan 2026?
You can meet our team of process-centric pharma experts live at the event in Milan. To ensure dedicated time with our specialists, we highly recommend booking a personalized meeting in advance via the registration form on this page.
How do Cegeka and Mavim accelerate Dynamics 365 implementations for pharmaceutical companies?
Cegeka utilizes standard industry-best-practice blueprints combined with the Microsoft Business Process Catalog inside the Mavim platform. This allows life sciences organizations to conduct visual fit-gap analysis workshops early on, drastically reducing implementation alignment time, safeguarding data integrity, and speeding up time-to-value.
How does the joint solution support GxP and regulatory compliance?
Our process-based approach maps compliance rules and operational workflows directly into a single system of record using Dynamics ERP/CRM and the Power Platform. This provides full traceability, precise production planning, and simplified quality control management required to meet strict global pharma standards.
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