We improve technical procedures and processes in the pharmaceutical industry, as well as administrative workflows. Short turnaround times guarantee stable planning and a competitive edge.
We adapt processes and workflows to new challenges for you. These can be production processes, where we use our own optimization methods to enable stable and fast production. They can equally be improvements to the supplier structure (“CMO Management”), internal order workflows, or other administrative processes.
We measure the process performance of the various workflows. These can be technical production processes or company processes such as CMO order processing, complaint management, and turnaround times in external laboratories.
The existing process is characterized within the joint team. We develop new solutions together and implement them together.
A few months after implementing the changes, check whether all desired effects have successfully occurred. We will correct the new process based on initial experiences.
Increase your throughput while simultaneously boosting your product quality.
Extract from FDA document
“Facilitate Continual Improvement
To identify and implement appropriate product quality improvements, process improvements, variability reduction, innovations, and pharmaceutical quality system enhancements, thereby increasing the ability to fulfill a pharmaceutical manufacturer’s own quality needs consistently. Quality risk management can be useful for identifying and prioritizing areas for continual improvement.”
Extract from FDA document
“Facilitate Continual Improvement
To identify and implement appropriate product quality improvements, process improvements, variability reduction, innovations, and pharmaceutical quality system enhancements, thereby increasing the ability to fulfill a pharmaceutical manufacturer’s own quality needs consistently. Quality risk management can be useful for identifying and prioritizing areas for continual improvement.”
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