Our quality commitment is very important to us.
For more than 10 years we have made a commitment to provide the highest quality analytical services and our employees are highly motivated and work strictly according to the GMP (Good Manufacturing Practice) guidelines and the ICH specifications (International Conference on Harmonization).
Moreover, we are in compliance with current pharmaceutical specifications and the associated laws and regulations.
Our highly qualified employees participate regularly in internal and external continuing education opportunities and they often travel to speak professionally at conferences and Workshops. SYNLAB Analytics & Services Germany GmbH is regularly monitored by the authorities in Cologne to maintain compliance as a pharmaceutical testing laboratory as defined by § 14(4) AMG with the GMP requirements.
Our lab and equipment are not only GMP-certified, SYNLAB Analytics & Services Germany GmbH in addition has been approved by the U.S. Food and Drug Administration (FDA).
Regular client audits ensure our analysis quality is consistent and we guarantee strict compliance with GMP guidelines based on pharmaceutical specifications for our clients in the pharmaceutical and biotechnology industries.
We perform analytical services using the most up-to-date science and technology based on the approved regulations and the applicable legal regulations.
The following links provide an overview of the most significant laws, guidelines and certificates that we follow::