MEDISCIS "“Medical Science Services” is a Clinical Research Organization situated over three different locations in France. We are capable of managing protocols from the traditional to the most complex and innovative.

We are an ideal partner for top level Pharmaceutical, Biotechnology, and Generics firms.

With established core competencies in Clinical Phase I & II trial Management, Bio-analysis, and Biometrics (Ph I-IV), our expertise comes into play at all stages of clinical research in the pharmacological and biotechnology fields, including:

• Clinical Development Support: TPP, Clinical Development Plan, Methodology, Bibliography, Sample Size, Budget Forecast, Study Outline
• Protocol Writing,
• Regulatory Submission Support,
• Drug Import and Release Management
• CRF Design and Printout
• Clinical Trial Preparation, Execution, and Monitoring
• Bio-analysis
• Biometrics (Data Management & Biostatistics)
• Pharmacokinetic Analysis and Report
• Full Study Report

The quality of this full project trajectory is maintained on account of a methodical internal Quality Control and Assurance program. Moreover, recent national and international regulatory guidelines are strictly followed to ensure the highest level of safety and quality.

Over 70 employees with professional Medical, Technical, and Business expertise incorporate their professional ethics, problem-solving tactics, and technological and project management expertise into each new project.

These attributes give MEDISCIS the ability to offer a tailor-made approach to management based on client needs and specifications. We pay attention to the details, while ensuring consistency, flexibility and reliability in our services. Give us a problem, and we’ll give you a tailor-made solution.”