We advise and support our clients in every area of pharmaceutical quality management as an independent service provider. Our many years of experience and high level of expertise allow us to support you comprehensively and sustainably. Read on and see for yourself.
GDP
Requirements for global supply chains are constantly increasing, also from a regulatory perspective. What are the implications that this has for pharmaceuticals producers and distributors in everyday life? How can you effectively implement Good Distribution Practice (GDP) Guidelines?
GMP
Quality assurance plays a crucial role in pharmaceutical manufacturing, because quality deviation can lead to serious consequences. What does GMP compliant quality management include? How will it be implemented into everyday use?
Qualified Person
The Qualified Person (QP) ensures that pharmaceuticals are manufactured in accordance with the Good Manufacturing Practice regulations and distributed in accordance with the Good Distribution Practice regulations, an extremely complex and demanding task.
Regulatory Services
Regulatory requirements in the field of medical devices are becoming more complex, boundaries between pharmaceuticals and cosmetics depend on many factors. Therefore expert knowledge and practical support are needed.
