PleaseReview CASE STUDY The Challenge Conducting clinical trials is a document intensive process, with all departments involved in the creation and review of documents related to submissions. These include protocols, reports, memos, certifications, contracts, quality agreements and clinical investigator agreements. In 2009, Amarin needed a solution that could simplify and speed up this process, especially as the Phase 3 trials had received FDA approval to proceed. Before PleaseReview, staff had circulated documents for review as email attachments or as hard copies for manual editing and review. However, a constant concern was that document confidentiality could be compromised. A key factor in their search for a review solution, therefore, was the ability to give reviewers secure

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