Empowering your success with quality solutions.
K-PHARM – GMP & GDP Pharma Consulting
Headquartered in DĂĽsseldorf, K-PHARM supports pharmaceutical companies in building compliant, and efficient quality systems.
With more than 17 years of expertise in GMP/GDP compliance, quality systems, audit readiness, and pharma operations, we deliver solutions that are aligned with your business goals.
We believe that a well-designed, company-specific Quality Management System is the foundation for product safety and long-term success. That’s why we focus on effective structures.
Our mission is to provide high-quality services while maintaining a commitment to social responsibility.
Our Services
Free Initial Consultation – 30 Minutes
In a non-binding call, we’ll take about 30 minutes to discuss your current situation, goals, and challenges.
What to expect:
A first professional assessment of your situation
Clarification of your specific question
Whether you're just exploring options or have a concrete project in mind – this conversation offers a clear starting point.
Completely free and without obligation.
GMP/GDP Compliance & Audits
We support you with internal audits, supplier evaluations, and inspections. With years of experience, we guide you safely and efficiently through every phase of the audit and inspection process.
Our services include:
Conducting GMP/GDP-compliant audits
Preparing professional audit reports
Inspection readiness support (e.g. EMA, FDA, local authorities)
Assistance with CAPA measures
Quality Management System & Project Management
We understand the importance of having a robust QMS in place and provide consulting services to help companies establish and improve their own QMS system, to develop and implement Quality Manuals with SOPs
Our services include:
SOP preparation or review
Staff training to ensure GMP/GDP compliance
Support with deviations, complaints, Change Controls and CAPAs
Reserve your appointment
Book your personal consultation now and take your project one step further.
Comprehensive, customized support
-
We offer professional GMP consulting to help pharmaceutical companies meet regulatory requirements and optimize their processes.
With extensive experience across all areas of Good Manufacturing Practice – from quality assurance and control to validation – we deliver practical solutions to your business.
Whether you need support with audit preparation, training, documentation, or process improvement, we provide expertise to help ensure your products remain safe and effective.
-
We support pharmaceutical companies in meeting GDP requirements across storage, transport, and documentation.
Whether launching new operations or improving existing ones, we help design efficient, compliant distribution and warehouse systems aligned with your business. -
We support you in building and further developing your GMP-compliant Quality Management System.
This includes the creation and implementation of quality guidelines, manuals, and Standard Operating Procedures (SOPs) – always aligned with regulatory requirements and the practical needs of your organization.
-
We support you throughout the entire process, whether it’s a regulatory inspection, internal audit, self-inspection, or a CMO audit.
-
We offer hands-on GMP/GDP training designed to ensure your team not only understands current requirements but can confidently apply them in daily operations.
Our training strengthens quality awareness, improves compliance, and reduces the risk of deviations.
-
Whether it's new process development or optimization – we support you through every phase of your project, from planning to execution and finalization.
-
Company evaluation is a critical part of any M&A process.
We conduct comprehensive assessments covering financial performance, regulatory compliance, and GMP compliance —providing the insights needed for confident decision-making.
Contact Us
Whether you have a specific request, a general question, or would simply like to learn more about our services – just use the contact form, and we’ll get back to you promptly.