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.