Regulatory Affairs

Our experts and partners can support you through the entire process. From the optimization of your initial specification or the consultation on pharmaceutical and medical legal requirements, throughout preparation and creation of application documentation all the way through to the market entry of your product - we support you with our profound competence, solid experience and personal accountability. You can be absolutely sure that all application and licensing procedures are completed GMP conform, efficiently and smoothly. The result is a marketable product product that meets the highest quality requirements. 




Any questions regarding your licensing and approval process? We look forward to hearing from you!



Product Development

Our experts are there to support you on the complex journey from inital product idea to the finished product.
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Product Transfer

We support you during your product transfer and ensure a smooth and efficient transition.
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Our state-of-the-art laboratories are equipeed with the most modern technology. Our specialists can analyze, evaluate and document your product in our own lab-data-system.
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Serialization & Aggregation

We are meeting the challenge of serialization by fulfilling digital (coding) and analog (packaging) requirements.
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