ECTD AND NEES
Compile your eCTD dossiers effortlessly with immaculate precision taking into consideration all the norms as framed by the regulatory authorities and fully compliant with ectd ICH module
CTD AND ACTD
Manage the documents in various formats (.doc, .pdf, .xml, .xpt, .xls and others) and also merge separate documents in one documents by one click. Single platform to manage, register, review, archive, publish CTD/paper dossier.
RIMS
RIMS software solution, is a centralized, platform that help manage global regulatory information across companies’ entire portfolio of products.
DRUG SAFETY
Streamline drug safety operations with a system dedicated to the management of Adverse Events related to pharmaceutical products with Advanced and AI driven Modules.
CLINICAL TRIALS AND BA/BE
An end-to-end solution suite which cater to the needs of clinical research project starting from Project Management, feasibility assessment, volunteer or patient enrolment using iris recognition technology, capture clinical trial data, multi-level review process, data compilation to data archiving.
