1. [Home](https://www.g2.com/) 2. ... 3. [Pharma and Biotech Software](https://www.g2.com/categories/pharma-and-biotech) 4. [AE Connect Discussions](https://www.g2.com/products/ae-connect/discuss) [ ![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_3d917fe2663f65e4f8d26a4d9a83b12b/ae-connect.png "Product Avatar Image") ](/products/ae-connect/reviews) [ AE Connect ](/products/ae-connect/reviews) 0 ratings AE Connect by QORO Intelligence is an AI-powered pharmacovigilance platform purpose-built for small and mid-size biotech companies. It streamlines the entire adverse event lifecycle from multilingual patient intake through structured triage, case management, and ICH E2B(R3)-compliant submission in a single, intuitive platform. With a seven-state triage workflow, role-based dashboards, and built-in MedDRA coding support, AE Connect gives pharmacovigilance teams the structure and visibility they need without the overhead of enterprise-grade systems. Regulatory submissions are formatted to meet FDA E2B(R3) requirements out of the box, so teams can focus on patient safety rather than formatting compliance. Whether you're a lean PV team managing your first IND or a growing biotech scaling your safety operations, AE Connect delivers enterprise-grade rigor at a size and price point that actually fits. Show More * * * ### 0.0 Nps Score Already have AE Connect? ### All AE Connect Discussions Search Most CommentedMost HelpfulPinned by G2Newest All DiscussionsDiscussions with CommentsPinned by G2Discussions without Comments FilterFilter Filter byExpand/Collapse Sort by Most Commented Most Helpful Pinned by G2 Newest Filter by All Discussions Discussions with Comments Pinned by G2 Discussions without Comments DS Loading... [Daman S.](https://www.g2.com/users/de784e3f-1714-4ea8-86f4-4421a3fb2c99 "Daman S.") • 3 months ago Founder, AE Connect by QORO Intelligence Inc. More Options - [ # What do small biotechs need to know about ICSR intake for the ICH E2B(R3) deadline? ](/discussions/what-do-small-biotechs-need-to-know-about-icsr-intake-for-the-ich-e2b-r3-deadline) The April 1, 2026 FDA deadline for mandatory ICH E2B(R3) electronic ICSR submissions is no longer on the horizon. It is here. If your biotech is still collecting adverse events on paper, in a spreadsheet, or through an unstructured email process, you have a compliance gap that needs immediate... 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Answer a few questions to help the AE Connect community [ Yes ](javascript:void(0))[ Yes ](https://www.g2.com/authorize?form=signup&return_to=https%3A%2F%2Fwww.g2.com%2Fproducts%2Fae-connect%2Fdiscuss%3Fsmall_ask%3Dae-connect) No ## Top Contributors in AE Connect 1 DS Loading... ### [Daman S.](https://www.g2.com/users/de784e3f-1714-4ea8-86f4-4421a3fb2c99 "Daman S.") Founder, AE Connect 2 pts