Being successful together!
We ensure the quality in the life cycle of pharmaceutical products with the help of our accompanying services in development, GMP-compliant manufacturing and inspection, and in the routine of market supply. Our outstanding GMP-knowhow allows us to develop and deliver tailored overall concepts for large-scale projects, and development, transfer and problem solutions in specialized subjects as well as in the traditional qualification and validation.
Through our services, we contribute to the development and availability of high-quality pharmaceuticals within a short time, which improves people’s quality of life.
We are Valicare – a global GMP service provider for pharmaceutical and biotechnology companies since 2002, with focus on the pharmaceutical qualification and validation sector and on GMP-requirements for novel cell and gene therapies.
Various customers – from startups to the large-scale industry – require tailored GMP-compliance solutions. We can implement small and large GMP projects promptly and are able to be flexibly available.
By using Life Cycle Management for qualification and validation, we enable our customers to comply with regulatory requirements throughout the entire manufacturing process and ensure compliance from conception to market launch.
Benefit from tailored plant integration and seamless processes, supported by our strategic partnership with our parent company Syntegon Technology.
With our help, your products can be brought to market in an efficient and safe manner!
Let us bring your products to market efficiently and safely!
Questions about…
- GMP compliance and consulting for cell and gene therapies
- Qualification and validation (life cycle management)
- Plant/line integration in partnership with Syntegon Technology
- Project management and regulatory support
- Audits and training
- Any GMP-related questions
We have the answers!