Your clinical trial. Your timeline
As we all know tight timelines is always an important requirement in all companies, and with the time constraints same tasks end up not being performed in time or important documents are not written with the desirable quality.
ITClinical's team wants to help you with the time managing, this is why we offer you a comprehensive range of services in scientific and medical writing.
We can assist you in all the documentation necessary to set up a Clinical Trial, from Standard Operating Procedures to Clinical Study or Pharmacovigilance Reports, without forgetting the essential documents as Study Protocol, Investigator Brochure, Informed Consent Form or Case Report Form totally adapted to our EDC system.
In addition to these study documents we also can provide you:
- Common Technical Document
- Scientific Publications
- Scientific Presentations
- Scientific Training Manuals
- Investigator's Brochure
Tell us what you need and we prepare an accurate, timely, and cost effective document with the highest ethical and scientific standards, because every document goes through a rigorous internal quality assurance process.
We are determined to provide you a cost-effective solution to fit your needs.Contact us