Integration Capable LMS for Better Compliance in Pharma

Be it the case of 429 inadequate standard operating procedures and document controls observation made by US FDA in 2018 or the fact that 25% of warnings made by US Office of Manufacturing Quality were for failure in maintaining written procedures and records, the cost of non-compliance is staggering, especially since Pharma operations are vast, at large scale and often involve contractual partners. Frowning at the cost of maintaining a team for document management and training personnel on SOP changes, doesn’t help. What helps is an LMS tailor-made for the needs of the pharma industry!

The very clear trend that has emerged from our research is that quality management (QMS) requires a robust document management system (DMS), and for every change in standard operating procedures, trainings must be rolled out to all impacted roles.

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