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.