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Our medical writing staff includes medical doctors with abundant clinical experience, research staff with years of experiences in pharmaceutical industries, and statistical consultants with good cooperations. The KLR team can develop scientifically and medically accurate documents and ensure full compliance with regulatory requirements. We can assist with a wide array of documents to support your clinical research at any point in development, including: ★ Product development plans ★ Non-clinical and clinical overview ★ Clinical trial protocols ★ Clinical trial reports ★ Investigator brochures ★ Patient safety narratives ★ Report Publishing Service ★ NDA materials to be submitted to authorities To date, KLR has provided medical writing services for Servier and two local companies regarding protocols and CSRs (Phase I and Phase III). In Sep 2014, KLR passed the review by a global CRO for phase I study report writing.
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