8 Quality
Management

We monitor quality processes for you or your suppliers. With higher quality, you create more stable processes and better products. This increases your added value.

MORE Overall quality depends crucially on the weakest link in the quality chain. We analyze your quality processes and those of your suppliers. We improve quality without creating a flood of new documents. This enables you to achieve greater added value.

Whether Good Manufacturing Practice (GMP) or ISO 9001, we manage your quality processes as an outsourced service or improve and optimize your own processes.

We increase the quality of processes and products. This increases your added value.

Contact one of our experts for a consultation and advice.

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Good Manufacturing Practice
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More power together Quality management is your advantage!

GMP and ISO 9001

Our experts are at home in both quality systems. This allows us to expand your quality system in a targeted manner and coordinate the various systems with each other.

Quality processes

We take over complete quality processes and manage them for you. Supplier management, complaints management, validations and transfers are processes that we can manage for you.

Business processes

We analyze your business processes to discover quality potential and make it available to you. This allows you to increase quality and added value together.

Process development, scale-up, process optimization

Unlocking potential

Increase your chances of success. Contact one of our experts for a detailed consultation.

Efficiency

Talk to one of our consultants about your challenge and your project.

Take your pharmaceutical processes to a new level - contact us and we will help you succeed!

Process validation

FDA note on the quality system

ICH Q10 describes one comprehensive model for an effective pharmaceutical quality system that
is based on International Organization for Standardization (ISO) quality concepts, includes
applicable good manufacturing practice (GMP) regulations, and complements ICH "Q8
Pharmaceutical Development" and ICH "Q9 Quality Risk Management."