I am Vanessa Montanari, Clinical Research Associate, Project Manager and Director, for 9 years, of Pharmaspecific, my own Contract Research Organization (CRO), in clinical research.
After 15 years of experience in clinical research, I had victories and failures. This guide is a summary of the lessons learned from this experience (project management, choice of provider, procedures, deviations, informed consents, ALCOA, SAE, inspections, enrollment, investigators, monitoring, patient reimbursement). I see all these aspects with you and give you all my feedback.
This guide will help you to carry out your clinical research projects successfully and in accordance with Good Clinical Practices. If you are a customer or future French customer, you will find all the necessary information including that applicable to France. If you are a foreign customer, you will see the aspect of international studies and also find aspects specific to France.
Good luck for your clinical trials. You can consult our website if necessary (www.pharmaspecific.com), and send me an email to contact[at]pharmaspecific.fr
Call us directly for any request for quotation on +33 (0) 987046492.
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Our collabor/Actors share their opinions. Watch our videos. Activate the subtitles in English.
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