Searching to optimize your time and human resources? In need of reliable and professional documentation for your presentations ? Short of time ?
PHARMASCRIPT is a company created in 2002 by Sandrine ROULOT-BOURGEAIS, Doctorate in Pharmacy (PharmD) Université Paris XI, Master in Statistics.
We offer more than 15 years of expertise in the pharmaceutical industries.
Located in Compiègne (Oise), 53 miles north of Paris, 37 miles from Charles de Gaulle Airport.
We understand very precisely the scientific questions you want to answer and draft documents with respect to your SOPs and templates always following international guidelines.
We write clear and specific protocols with all the information necessary for a fair and consistent implementation of your study.
We create CRFs with the requirements of your protocol in mind and completely collect and organize all relevant patient data to ensure quality control.
We prepare information forms and informed consent forms that are accessible to patients, allowing them to make an informed decision based on objective and accurate information of your product and of the clinical trial, highlightening all risks and potential benefits.
We carry complete Investigator's Brochures (IB) containing all available data on the product development, to investigators and ethics committees.
We draft comprehensive study reports detailing the story of your clinical study, its results, and its contribution in the medical field in compliance with ICH E3, and your SOPs and templates.
We write reports on any subject required (ex. clinical trial results, literature review, Expert Reports, pathology, management...) in partnership with the authors that you have chosen. Through us, you will deliver a fair and controlled summary to the medical world. Our expertise allows us to obtain the agreement of reading committees in 100% of cases after only few comments from reviewers.
Feel free to leave us your contact information and we will be happy to respond as soon as we can.