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Ergomed has a global team of experienced, native speaker Medical Writers, both in-house and consultants that are available to assist in the development and writing of all your study documents from Protocol and the Patient Information Leaflet / Informed Consent Document, all the way through to the final production and publishing of your final clinical study report. Ergomed MW has robust processes leading to high quality documents within the fastest timelines, that our detailed in our SOPs, and in-house templates that have been developed to comply with ICH GCP and are updated to follow all new requirements and guidance, although we are always open to utilising our clients templates if that is their preference.
The Ergomed Medical Writing team is also available to review, QC and consult on all documents for our clients. Ergomed’s team consists of medical and regulatory writers across multiple time zones that work alongside and are supported by Ergomed Physicians, Medical Monitors, Statisticians, Data Management, Regulatory Affairs and Quality Assurance.