On Demand Webinar – Accelerate Your Submission Content Preparation Opportunities in Technical Compliance
A webinar sponsored by Astrix Presented by: Laszlo Rivnyak, Business Analyst and Key-Account Manager, DACHS Computing & Biosciences GmbH & Gabriella Varga, Business Analyst, DACHS Computing & Biosciences GmbH Overview Submitting on time and completely in compliance with regulatory agency requirements is difficult. This webinar explains how businesses can speed up content preparation processes for […]
Enable Your Drug Development CMC Digital Transformation Strategy with a SCDM Guided Workflow System
Overview The Chemistry, Manufacturing, and Controls (CMC) Module 3 component of the Common Technical Document (CTD) required for pharmaceutical regulatory submissions requires extensive documentation, including drug substance and drug product information, manufacturing processes, analytical methods, stability studies, and more. Managing the manual transcription and compilation of this documentation consisting of text annotations, images, data, tables, […]