Clinical Development

Starting on the right foot is crucial.

Start your trial with confidence/peace of mind.
An individual view on your clinical trial in the early Phases (Phase I including first-in-man/first-in-patient – adaptive Designs) is essential for successful drug development.

In addition to in depth experience, especially in oncology, you‘ll also find first class international regulatory affairs services at AMS.  

 

Design the most effective trial for quicker approval.

Read more or find out how AMS Clinical Research services can meet your needs:

Get in touch with us at:

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• 2011 – AMS AMNOG Services pioneer • 2013 – AMS-Investigator SELF-TRAINING PORTAL • 2013 – “BEST CRO” by one of ther world’s Top 5 Pharma companies’ CRO Evaluation for AMS – Clinical Operations Services • 2014 – AMS performs Medical App Studies including eCRF-data integration • 2015 – AMS Medical Science is awarded “Provider of the Year, worldwide” the world’s Top 10 Pharma companies • 2015 – AMS develops an E-feasibility tool • 2015 – Innovative Tool for Patient Reported Outcomes: AMS-ePRO (BYOD-type PRO solution) is developed • 2016 – AMS – Regulatory Affairs is nominated on the short-list for TOPRA Award for Regulatory Excellence

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