Document Authoring, Review and Approval are key business processes in the Life Sciences domain covering the Biopharmaceutical, Medical Devices and Cosmeceutical industries.
From Product Briefs to Clinical Study Protocols and Summary Reports, from Safety Aggregate Reports to Systematic Literature Review reports, Label documentation to SOPs – document authoring is often collaborative and requires inputs/approval from multiple functions.
Information that goes into a section is frequently available only in unstructured formats and department-internal file folders or systems.
Life sciences professionals are drowning in paperwork because the current systems are not tailored to their needs.
Precious SME time is spent on document administrative tasks such as collating information, formatting the document, maintaining multiple versions of a document, waiting for review comments to be resolved etc.
It’s nearly impossible to collaborate internally or externally with other professionals without spending hours, if not days, making sure that the documents are accurate.