Development of medical documents

Development of Investigator’s Brochure;
Development of Study Protocol;
Development of Patient Information Sheet;
Development of Informed Consent Form;
Development of Standard Operational Procedures;
Development of Product Efficacy and Safety Summary;
Development of General Study Report.

We will not only develop the documents associated with clinical studies but also analyze the documents available (nonclinical reports, references) and provide you with a summary report on further actions, for example, whether you need a clinical study, its size and particularities.