Integration and Adaptation Services

Process Automation and Optimization Propelling Economic Growth!

Your pharmaceutical company is experiencing continuously increasing pressure to optimize productivity.
Your requirements regarding the development and realization of efficient production processes are increasing.
Entirely new processes have to be developed as a result of adding potential new active ingredients.
This results in a massive rise in samples and analyses, which in turn results in a significant rise in data, particularly with regard to the new PAT-initiative of the FDA.

Existing heterogeneous laboratory equipment, with a resulting complex IT-environment, as well as increasing demands on quality management and quality assurance are causing work routine and production processes to slow down more and more.
Necessary quality assurance procedures constrict the flexibility of your work routine and make it difficult to keep track of the continuously increasing volume of data.

We support you in handling the above-mentioned challenges, in order to meet regulatory requirements. At the same time we provide you with a better overview of your over-all processes. A competent team of IT, QM and scientific specialists will develop solutions for data integration, communication and archiving interfaces, customized according to your requirements in consideration of all cGMP relevant aspects.

We are able to individually adapt our cell culture analysis systems to your processes. Any information available is processed target-oriented into significant analysis data.

Your Benefit:

The majority of projects in which our solutions have been put into effect were proven to be worthwhile less than a year after implementation. You are able to focus on essential processes while we optimize your quality and information management!

Possible Project Scenarios:

Programming of interfaces for:

• exchange of heterogeneous laboratory equipment data
• link of laboratory equipment to LIMS / LIS software, tools for archiving or databases

Individual development of:

• tools for data interpretation
• components for process control or warning systems etc., etc...

Central databases for:

• corporate internal alignment of data (global and spanning multiple locations)
• central and inter-group data analysis
• demand-driven evaluations

Strategic Proceeding

• combined analysis of requirement and application
• project planning
  • URP (user requirement phase) - your wish list
  • FSP (functional specification phase)
  • DSP (design specification phase)
• professional ongoing project "on side" and "offshore" support
  • transparent project management
  • interfaces for communication to all project partners
  • permanent project control
  • cGMP compliance
  • efficient product launch by qualified and experienced personnel
  • success monitoring at regular intervals