Resource Library
Our library offers actionable compliance tools and templates covering risk management requirements for life science organizations, post-market commitment and surveillance, clinical affairs, site and evidence planning, labeling and UDI requirements, submission guidance including applicable checklists, and by enabling Regulatory & Quality teams access to concise information operationalizing global regulatory obligations and mitigating recurrent review processes, streamlining regulatory compliance, intelligence and science requirements with global health authorities.
Novo Compliance’s Resource Library provides information for our clients related to global regulatory frameworks governing pharmaceuticals, biologics, and medical devices, on various pathways required by major authorities including the FDA, EMA, MHRA, PMDA, TGA and WHO, providing harmonization with regulations, guidance’s common specification and consensus standards advancing marketing access.
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