Über uns
Who we are
Pharmalog joined Astrum CRO in 2023. 25 years of combined clinical excellence
Our philosophy since 1983 and further on is based on transparency, accuracy, flexibility and approachability, values that drive both, our cooperation with our clients and cooperation among ourselves. The studies are naturally conducted according to high ethical and scientific standards and in accordance with the principles of good clinical practice (GCP).
With more than 450 successfully conducted clinical studies for over 80 companies, we are experienced in many different areas of indication.
Since 2011 we are an audited member of BVMA [Federal Association of Contract Research Organisations], which isthe official representative of German CROs. In this role, the BVMA represents the interests of its members in the EUCROF - the European CRO Federation.
As part of GXP compliance, which applies to manufacturers and service providers in the pharmaceutical industry, our computer systems are validated in accordance with GAMP5 guidelines.
Since 2012 our quality management is audited annually with regard to its function within the framework of ISO certification, whereby the greatest priority is given to continuous improvement.
Our Pan-European team of more than 300 employees, offers a wide range of skills from dynamic, highly-trained professionals across our offices in France, Germany, Portugal, Spain, and beyond.
At Astrum, we offer a full range of clinical development services spanning the entire drug development life cycle. Our client-focused approach coupled with our size means we can deliver end-to-end services or stand-alone solutions that are fully tailored to our client’s needs.
Our ability to adapt to the specific requirements of each project, maintaining focus on every detail, while always keeping sight of the bigger picture, ensures that we provide optimal solutions for our client
