After the Clinical Study

Clinical Study Reports (CSRs Phases I to IV)

Our specialized Clinical Study Report (CSR) writing team will prepare your document in accordance with ICH standards and ensure that it follows the standard format used by your company. Precision and consistency are guaranteed: all of the clinical trial documentation produced by Synergy Pharm is subjected to our quality control procedure, undertaken by another experienced medical writer in our team.

Lay Summaries

Authorities in Europe are now asking sponsors to publish a summary of the results of their clinical trial that is intended for lay persons. Our team has the specific skills required to write your lay summary.