Go back to MDS Pharma Services home page

Skip Navigation LinksHome / Services / Global Clinical Development / Medical and Scientific Writing
Medical and Scientific Writing


MDS Pharma Services offers a fully flexible range of medical and scientific writing services. Our medical writers can provide a stand-alone service, collaborating with our client's project team to write or review a clinical study report, protocol, patient safety narratives, manuscript for publication, or periodic safety update report. Our resources can be utilized as part of a full service project, and assist in the regulatory submission process with integrated summaries of safety, integrated summaries of efficacy and electronic regulatory submissions.

MDS Pharma Services' medical writing team follows our global standard operating procedures (SOPs) to ensure that protocol and clinical study report development are performed in a consistent manner throughout the company. SOPs and templates provided by the client to our team of medical writers would supersede those of MDS Pharma Services. The requisite International Conference of Harmonisation's (ICH) guidelines are also utilized to ensure that the document provided meets the standards required for regulatory submission.

Our team of medical writers based in France, Spain, UK and USA is dedicated to delivering high quality output, with full documentation and review at all stages. With proactive input, ongoing involvement and effective communication throughout the project, the medical writing department at MDS Pharma Services will provide timeliness, accuracy and integrity to your clinical programs.

Skip Navigation Links.

© 2009 MDS Pharma Services     |     Corporate Governance     |     Legal     |     Privacy     |     Site Map