Quality of Life Research CRO is a company dedicated to comprehensive planning and organization of phase I – IV of clinical trials, prior to the executive part we offer drawing up and preparing documentation that is essential to conducting clinical research, such as: patient informed consent form, CRF as well as medical records. Appropriate planning of the study and well-prepared documentation are the key elements contributing to the proper conduct of the entire process. That is why we make sure that our customers are provided with high-quality documents which are optimized, internally consistent, and compliant with standards, so as to avoid any potential problems in the course of clinical trial. We also provide support in the preparation of the final report. Depending on our clients’ needs, we may create documents in different languages, adapting them to the local requirements.