Part of US based
Semler Group of Companies,
in business since 1946


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Medical Writing

Semler Research Center's medical and scientific writing group provides expert regulatory and medical writing services developed with the insight that each document we generate is an integral part of a much wider clinical-regulatory documentary process impacting the development of your product.

Our cross-functional team of physicians and scientists is highly experienced and has met or exceeded all client agreed deadlines over the last 4 years. Our group's track record of working with pharmaceutical and biotechnology companies in pharmaceutical development, clinical development and manufacturing sectors brings broad perspective and understanding of the development process which forms the basis for document authoring.

Our expertise ranges from clinical-regulatory documents required to support product labeling, clinical study protocols/amendments, ICDs, investigator brochures and clinical study reports and patient narratives right up to the authoring of eCTDs. We additionally offer wider-scope writing services including authoring of manuscripts and other post-marketing documents.



About This Service

SRC offers comprehensive Phase I-IV services for drugs, devices & diagnostics.  The team is well-entrenched in regulated market requirements & GCP. Our collective goal is to shrink your time-to-market through superior scientific expertise and trial management innovation.