Organizations face strategic issues of sales and marketing practices and decreased product life cycles as well as privacy of patient and customer information.
LogicERM provides a customizable framework to address the needs of pharmaceutical and biotech companies to manage their clinical trial vendor reviews, clinical practice and performance improvement, regulatory compliance process and facilitate risk analysis, business operations, audits and resolution of findings. Regulatory requirements include FDA GXPs and reporting mandates, international drug safety standards, and cross-industry compliance requirements stipulated by laws such as Sarbanes Oxley Act (SOX). LogicERM brings together risk management, compliance, business continuity, continuous performance improvement as well as related communication, analysis and reporting under a common platform.
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