It is a legally mandated obligation for each pharma company to track PV agreements and contracts relating to pharmaceutical products and the exchange of Adverse
Deal with incoming Medical Inquiries and information requests via call centres, emails, and more. Real-time searching for answers, including automatic sending, and full per-country data
Ensure the data in your CARA Life Sciences Platform meets the standards and norms of the MedDRA dictionary / thesaurus.
Revolutionise clinical trial management with an integrated eTMF on the CARA Life Sciences Platform. Our eTMF solution offers comprehensive, DIA reference-model based documentation management, automated
With today’s need for speed and efficiency in the life sciences industry, Regulatory Affairs, Pharmacovigilance, Clinical Research, and Quality Management cannot operate as independent islands
Gone are the days when Regulatory Affairs, Pharmacovigilance, Clinical Research, and Quality Management could operate as independent islands within a pharmaceutical organisation. With todays need
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