workflows , have a central content repository , audit trail for records , version comparison and overall led to improved speed of compliant content at scale . They now generate more than 10,000 promotional content annually .
What trends do you foresee shaping the future of the life sciences and healthcare sectors in India , and how is Veeva Systems positioning itself to address these trends ?
India is a key strategic market for life sciences companies , with its own unique challenges around access , speed to market and fast-changing HCP expectations . In response , biopharmaceutical companies are upgrading their goto-market models by enabling new data & digital capabilities . Veeva Systems is investing in solutions that help life sciences organisations in India adhere to evolving regulations while streamlining processes , ensuring efficiency without compromising compliance .
Veeva recently unveiled Vault CRM , the next generation of CRM for life sciences . Built on the Veeva Vault platform , Veeva is the first and only company to offer a common platform across our Commercial and R & D suites of applications . This enables biopharma companies to bring commercial sales , medical and
“ Integrating cloud-based technologies will bring about a paradigm shift in life sciences and healthcare organisations .”
marketing functions together with product development , including clinical , regulatory and quality data . With a connected ecosystem from development to commercialisation , companies can seamlessly share information between teams while maintaining control and ensuring compliance .
To enable efficient quality management of products manufactured , Veeva ’ s Quality Systems Vault Quality Suite unifies quality systems and processes on a single cloud platform . Quality Suite applications exist within a single Vault , which allows for the consolidation of quality processes that were traditionally managed in siloed , disparate systems . Within this , the Vault QMS manages and tracks quality processes such as deviations , complaints , CAPAs , change controls , audits , and risk management , while the Vault Validation Management is a paperless validation solution that optimises the end-to-end validation lifecycle process , digitalising processes that were historically paper-based . Use of these can help organisations manage submissions faster to international regulators . Such a digital transformation can further strengthen the companies supplying drug products to international markets .
BioTech
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