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.
Good Manufacturing Practice (GMP) is the basis for this. GMP is not enough for efficient processes. Quality by Design (QbD) and Design of Experiments (DoE) bring high added value and accelerate processes.
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.
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.
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.
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.
Increase your chances of success. Contact one of our experts for a detailed consultation.
Talk to one of our consultants about your challenge and your project.
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."
