Salogic is an AI platform for quality teams in pharma, medical devices, clinical research and food and beverages.
It investigates quality events, reviews and digitises documents, and flags compliance risk early. Your QA team reviews and signs off every step.
Built in Australia for TGA, FDA, EU GMP and PIC/S.
About Salogic Technologies
Driving Innovation in GxP Compliance with Artificial Intelligence
Based in Australia, Salogic Technologies is at the forefront of developing AI-powered software solutions for highly regulated industries such as pharmaceutical, food & beverage, and medical devices. Our mission is to empower organizations worldwide to achieve and maintain GxP compliance with unprecedented efficiency and accuracy, allowing them to focus on innovation and operational excellence.
We leverage advanced AI and machine learning algorithms to transform complex compliance processes, providing intelligent automation and actionable insights. Our flagship GxP Compliance product is designed to minimize risks, reduce operational overheads, and enhance the integrity of your quality management systems.
AI-powered insights for GxP
Meet the Team
Combining deep domain expertise in life sciences compliance and cutting-edge artificial intelligence.
Ish
CEOChief Executive Officer & Co-Founder
Steering strategic direction, commercial growth, and industry partnerships. Dedicated to transforming regulated quality operations into a continuous competitive advantage.
Den
CTOChief Technology Officer & Co-Founder
Leading platform architecture, engineering, and enterprise AI innovation. Focused on building secure, audit-ready AI workflows engineered for rigorous GxP environments.
Quality teams are stretched thin
Investigations, document control and risk tracking still run on spreadsheets, email and memory. The work is slow, the evidence is scattered, and issues are often found by an auditor first.
Investigations drag on
Quality events take weeks to close. Root causes default to “human error” and the same issues come back.
Documents drift
SOPs fall out of step with regulations and with each other. Paper and legacy records stay locked away and unsearchable.
Risk is seen too late
Signals sit in separate systems. Overdue CAPAs, training gaps and supplier trends surface during the audit, not before.
Key Capabilities
Empowering Your Quality & Regulatory Compliance Journey with Advanced AI
AI Compliance Assistant
Ask a question in plain English and get an answer from your SOPs, past deviations and CAPAs, validation documents and FDA, EMA and TGA guidance, with a link to the exact source.
- Every answer cites its source
- Follows each user’s access rights
- Your data is never used to train models
Intelligent Document Management
Check an SOP before it goes for approval. Salogic flags missing sections and unclear steps, explains what changed between versions, and checks the document against the regulation or standard you choose.
- Finds gaps: missing roles, undefined terms, steps with no record
- Plain-English comparison between versions
- Checks against GMP or ISO 13485 requirements
- Suggested document classification
Risk-Based Compliance Monitoring
See where your next audit finding is coming from. Salogic watches the signals auditors check (overdue CAPAs, repeat deviations, open changes, training gaps and supplier issues) and scores each site, line and product.
- A risk score with the reasons behind it
- Heat map for management review
- Alerts when a CAPA goes overdue or a deviation repeats
- Connects across training, change control and supplier data
Intelligent Document Extraction
Turn scanned batch records, logbooks and legacy PDFs into searchable data. Every extracted value links back to the page it came from, so a reviewer can check it.
- Reads scanned batch records and forms
- Flags missing signatures, dates and entries
- Every value traceable to its source page; originals unchanged
- Feeds the quality assistant and risk monitoring
Quality Event Management
Log a Quality Event in minutes. Salogic suggests the category and severity, finds similar past events and routes it to the right reviewer. Your QA team confirms each step.
- Suggested classification and severity
- Similar past deviations surfaced automatically
- Routing to the right reviewer, with due-date tracking
- Also handles food-safety non-conformances and clinical protocol deviations
Root Cause Analysis (RCA)
Get past “human error”. Salogic guides each investigation with 5 Whys, and pulls in evidence from past deviations, batch records and SOPs.
- Challenges weak root causes
- Evidence linked to each cause
- Investigation report drafted for QA review
Corrective and Preventive Actions (CAPA)
Turn root causes into actions that work. Salogic suggests corrective and preventive actions, tracks them to closure and checks they worked, flagging when the same problem comes back.
- Actions linked to the root cause
- Owners, due dates and overdue alerts
- Effectiveness checks with set criteria
- Alerts when a closed CAPA’s problem comes back
Global Impact from Australia
Serving Innovators Across Continents in Regulated Sectors
While proudly headquartered in Australia, Salogic Technologies is built for the global stage. Our GxP Compliance solutions are designed to meet diverse international regulatory requirements, supporting companies in diverse regulated sectors across every major market. Join our growing list of partners worldwide.
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Latest Insights & Industry Articles
Explore expert articles, regulatory insights, and industry best practices to accelerate your GxP quality and compliance operations.
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