The experience of the previous years testifies, modern studies are becoming more and more complex, extensive and demanding. In order to keep up increasing demand, the study sites need to be continuously optimised or adapted. To source qualified and trained personnel and those that are adequately qualified that can be trained, to properly prepare and keep documents up to date, to be constantly present in the international clinical research market and to endeavour to access and research the up-to-date information on drug development and to proactively show that your interest in clinical trials is in the right place are only some of the challenges that we master daily together with our sites.
As a professional Site Management Organization (SMO) we support your site from the beginning on the way to solving your individual issues and strengthing your existing position or establishing you as a qualified study site. In our work, we see ourselves as a voice of the study sites, which directly communicates arising problems and requirements with the right contact persons and acts as a bridge between the pharmaceutical companies/CROs and your site.
As our partner you will profit from our experience and contacts to renowned clients and pharmaceutical companies, who take advantage of our network of established study sites with various indications.
We will help answer the question of how a study site is chosen by contractors or how you can start working as a study site. Take a look at our page and then feel free to get in touch with us. It will be exciting!
Yours Helena Sigal
If you have not found the right answers to your questions on our website, then do not hesitate to contact us for information about our possibilities and offers.
SIGAL SMS GmbH
Egelstraße 4
04103 Leipzig
Tel: +49 (0) 341 962 800-0
E-Mail: kontakt@sigal-sms.de