BiologicsMD provides a cloud‑based platform that centralizes experimental, manufacturing, and regulatory data for biologics development, creating a unified workspace for scientists, engineers, and compliance teams. The system offers automated workflows, predictive analytics, and role‑based security with audit trails, while integrating via APIs with existing LIMS, ERP, and ELN solutions to streamline collaboration and support FDA 21 CFR Part 11 compliance.
Funding
$58.1K raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Biopharmaceutical companies and research institutions often struggle to efficiently manage complex biologics development data, leading to fragmented workflows, data silos, and delayed decision‑making across discovery, manufacturing, and regulatory processes.
Solution
BiologicsMD offers a cloud‑based platform that centralizes biologics research and development data, providing a unified workspace for scientists, engineers, and regulatory teams. The system integrates experimental results, manufacturing parameters, and compliance documentation, enabling real‑time collaboration and traceability. Built‑in analytics and workflow automation help users identify critical path bottlenecks, predict manufacturing outcomes, and ensure data integrity for regulatory submissions. Role‑based access controls and audit trails maintain security and meet industry standards, while API connectors allow seamless integration with existing laboratory information management systems (LIMS) and enterprise resource planning (ERP) tools.
Target Audience
Primary customers are biopharma companies, contract manufacturing organizations, and academic research labs that develop therapeutic proteins, antibodies, and other biologic products.
Features
- Centralized repository for experimental, process, and regulatory data across the biologics lifecycle
- Automated workflow engine for protocol execution, review approvals, and change management
- Integrated analytics dashboards with predictive modeling for yield and stability forecasting
- Role‑based permissions, audit logs, and compliance reporting aligned with FDA 21 CFR Part 11
- RESTful APIs and pre‑built connectors for LIMS, ERP, and electronic lab notebook (ELN) systems
- Secure, multi‑tenant cloud architecture with data encryption at rest and in transit