M.Sc. | Dipl. oec. troph. (FH)
Christian Reinfelder
CEO
VITA
Experience:
- 25 years of experience in management consulting
- 20 years as a lecturer in quality management at Fulda University of Applied Sciences
Expertise:
- Certification body manager
- Head of Quality Management and QMB
- Project manager and leader
- Lead Auditor
- Trainer
Passion:
- Digitalization and sustainability

Business continuity management: How companies strategically secure their resilience
In a world where disruption has long since become the norm, business continuity management (BCM) is no longer an option, but a necessity. Whether cyber attacks, natural disasters, supply chain disruptions or IT failures: Crises affect companies…

Continuous manufacturing: future trend in the pharmaceutical industry
The pharmaceutical industry is at a turning point. For decades, traditional batch processes characterized the production of pharmaceuticals. Although these have proven their worth, today they are often considered rigid, slow and resource-intensive.…

How to create an effective quality management system (QMS) in accordance with ISO 9001
A quality management system (QMS) in accordance with ISO 9001 is much more than a formal set of rules - it is a strategic tool that companies can use to make their internal processes transparent, reliably meet customer expectations and build…

ISMS 2024: What companies need to know now about NIS2, DORA, CRA and ISO/IEC 42001
The demands on information security are increasing rapidly and with them the regulatory pressure. Cyber attacks such as ransomware, supply chain attacks and targeted attacks on critical infrastructures have long been part of everyday life.…

Enhancing Process Stability through Effective Deviation Management
Focus topics: Deviation Management, Process Stability, CAPA, Regulatory Compliance, Operational Excellence In today's fast-paced, highly regulated industries, maintaining process stability and ensuring product quality are paramount. Deviation…

Untrue Supplier-Audit Reports: The Danger of Ethnocentric GMP-Auditing
If You are in any QA / QU role and are responsible for audits and audit reports in the GxP-context, I encourage You to take time and read this, it will be worth Your while. And if You are a QP (like I have been), this is likely to help You.…

Insights into our project experience: Successful implementation of quality assurance agreements (QAA) in the pharmaceutical industry
As part of a project for a pharmaceutical manufacturer and its contract manufacturer, we demonstrated our expertise in the implementation of quality assurance agreements (QAA). The aim of the project was to optimize the quality assurance processes…

GMP standards for medicinal cannabis: guaranteeing quality in an emerging industry
The medical use of cannabis is gaining increasing recognition and legal approval worldwide, leading to growing demand and increased regulation. In this dynamic environment, Good Manufacturing Practice (GMP) standards are crucial for the production…

GxP audits: How important are they and how are they conducted?
In the highly regulated pharmaceutical industry, audits are more than just a control mechanism - they are an indispensable tool for ensuring the quality and compliance of processes. Audits play a key role in ensuring that companies adhere to…




