Qualitum
Qualitum is an agentic platform for computer system validation (CSV/CQV) in regulated life-sciences. It drafts IQ/OQ/PQ protocols, GAMP 5 classifications and audit trails straight from source documents (URS, P&IDs, SOP libraries), with every requirement traced end-to-end through a queryable graph that replaces spreadsheet RTMs. All ALCOA+ data-integrity criteria are monitored on every record, not samples, with humans reviewing and approving agent output. Qualitum runs single-tenant on AWS, Azure or on-prem, with customer-managed keys and no training rights on customer data, and connects to systems of record already in use (Veeva, MasterControl, TrackWise, AVEVA PI, Tulip and others). Built for Heads of Validation and validation consultancies at pharma, biotech and medical-device companies. Annual per-site licence, quoted on request; an 8-12 week fixed-fee pilot (one system) is available.
Learn more
Labguru
Labguru is a secure, cloud-based Electronic Lab Notebook (ELN), LIMS and informatics platform which offers a complete solution for life science research and industry. It records and manages laboratory data and inventory, includes molecular biology tools and chemistry tools, enables automation of the lab, insight into lab data making labs run more efficiently.
With Labguru, scientists can design experiments and workflows, capture structured and unstructured data, manage projects, and share their work. Customizable experiment templates, integration of protocols, SOPs, and other cutting-edge features help to increase data quality, streamline workflows and reduce costs. Labguru is available on desktops and mobile devices via the cloud.
Labguru is part of Holtzbrinck Publishing Group and serves over 100,000 scientists worldwide from startups, universities, research institutes up to some of the largest pharma companies.
Learn more
Merit for Life Science
Cloud-first ERP is intentionally tailored for life science organizations. Merit for Life Science is cloud-first ERP purposely built for biotech, pharma, and medical device manufacturers. It advances Dynamics 365 finance and operations to connect your entire organization. Mapping resource qualifications to production requirements. Monitoring vendor relationships in procurement to help ensure quality standards are met in manufacturing. Providing your life science organization with visibility and transparency to deliver safe, innovative products and much more. Your organization has unique needs and we understand them. Get the full picture of what we offer. Delivering an industry-tailored solution that meets the rigorous requirements of pharma, biotech, and medical device companies. Improve your decision-making process with reliable, auditable accounting practices. Establish financial reporting standards for acquired entities or prepare for acquisition.
Learn more
Qualcy QMS
Qualcy Bio-Med QMS Software has been designed for Bio-Medical companies (including Biotech, Pharma and Medical Device) to manage QMS records for ISO13485 and FDA requirements. * Designed for meeting the requirements for 21 CFR Part 820 * Has built in features for E-sign, audit trails and complies with 21 CFR part 11 requirements. This software helps manage the records for Doc. change control, complaints, audits, CAPA, NC Records, Training Records and more.
Learn more
