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:

ClinicalResearch bottom

• 2011 – AMS AMNOG Services pioneer • 2013 – AMS-Investigator SELF-TRAINING PORTAL • 2013 – “BEST CRO” by one of the 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” by one of 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

Meet us at a conference

News

  • EMA-EUnetHTA Parallel Consultation

    Artikel vom 01 August 2017 News

    Profit from the simultaneous feedback of regulatory and HTA bodies in order to generate your data set in the most efficient way! What is new? EMA and EUnetHTA h... weiterlesen
  • AbbVie TRIUMPH AWARD 2015

    Artikel vom 24 Juni 2016 News

    Um Kooperationen auszuzeichnen und Partner entsprechend zu honorieren, verleiht AbbVie Global jährlich den Preis 'Supplier of the Year'. Kriterien, um für den P... weiterlesen
  • AMS ePRO

    Artikel vom 01 Juni 2016 News

    The aim of the AMS -ePRO system is to enable patients to enter online (on their own smartphones, tablets or computers) their health related data in response to... weiterlesen