The number of clinical trials as well as the amount of regulatory documentation required for each trial is increasing. The production of high quality documents within strict timelines is therefore resource intensive and demanding. By using Kinapse’s standalone QC services clinical trial sponsors can increase the quality of clinical trial documents while accelerating timelines.
Kinapse has provided standalone QC services to the pharmaceutical industry for over 8 years. Our team of QC specialists have reviewed over 3600 regulatory documents achieving 100% on-time delivery.
Our experienced, dedicated and scalable QC team is ready to address challenges caused by poor document quality; reducing the number of review cycles, staff workload and delays to regulatory approval.