XEVMPD, EVPRM
Populate Medicinal Product Report Message having information of authorized medicinal products and approved substances in EVMPD (EudraVigilance Medicinal Product Dictionary).
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EDC, eCRF for Clinical Trials
Managing clinical trial progress, planning, monitoring activities and maintaining investigator information and barcode generated screening and registration becomes easier with the use of BizNET-CTM. An intuitive, user friendly...
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eCTD Dossier Life cycle
Compile your eCTD dossiers effortlessly with immaculate precision taking into consideration all the norms as framed by the US FDA, UK MHRA, EU v1.3 or v1.4 and similar regulatory authorities with KnowledgeNET...
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Pharmacovigilance software
PvNET is a pre- and post- marketing adverse event reporting (ADR) software which fulfils the requirements of 21 CFR Part 11 compliance and the regulatory authorities simplifying CIOMS, CIOMS II Line Listing and MedWatch generation...
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News
1. EVPRM submission, EVPRM solution
2. SPL R4 is in news these days!!
3. Pharmacovigilance
4. eCTD EU module-1 v1.4
5. eDMF approved by US FDA
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Blogs
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EMA: New eCTD Validation Criteria (v3.1) and NeeS Validation criteria (v2.1) Effective from 1 September 2011 |
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All Blogs |
PPTs, Word files, Brochures and other content and related links to various Subjects and Topics.in detail... |


