drug manufacturing software
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N-SIDE Suite - Game-Changing SaaS Platform
The N-SIDE Suite is a game-changing SaaS platform supported by a team of industry-leading experts. ...
By N-SIDE based in Louvain-La-Neuve, BELGIUM.
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RegScan - Version MDR - Medical Device Reporting System
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the device manufacturer, and ...
By RegScan, Inc. based in Williamsport, PENNSYLVANIA (USA). from Quality Suite Checklists Software line
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Eviti Connect - High-Value Autoimmune Care Diseases
Reimburse High-Quality, High-Value Autoimmune Care with Confidence. Providers don’t want to delay patient care. Payers don’t want to waste money on unwarranted, ineffective autoimmune care. Both want to improve clinical outcomes while ensuring healthcare dollars are spent ...
By NantHealth, Inc. based in Morrisville, NORTH CAROLINA (USA). from NantHealth Eviti - Eviti for Oncology Software line
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Freyr SPL-SPM - Structured Product Labeling/Monograph (SPL-SPM) Software
and content of label information as required by the United States Food and Drug Administration (US FDA) and Health Canada. The US FDA has mandated SPL requirements for over 50 types of documents, and HC has mandated SPM requirements for over 6 types of ...
By Freyr Solutions based in Princeton, NEW JERSEY (USA).
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