Owlytic Audit
Who Is the Company Behind Owlytic Audit?
- Seller: Owlytic GmbH
- Year Founded: 2023
- HQ Location: Bad Rappenau, DE
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LinkedIn® Page: www.linkedin.com
2 employees on LinkedIn®
Total Products under this Category: 315
Last updated: September 01, 2026
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Oxialoffers interoperable software modules for the comprehensive management of risk, internal control, and internal audit.
P3AUDIT helps organisations reduce the time they and their supply chain spend on compliance admin, and eliminates avoidable process errors that lead to regulatory penalties and operational disruptions. P3AUDIT guides users with compliance requirements, leveraging AI to automate the capture, validation and mapping of evidence across their team, SOPs, and suppliers: giving real-time visibility and control over compliance postures across complex regulatory environments, identifying risk and building resilience to data breaches and other forms of business disruption. Who We Serve Regulators, regulated organisations, and regulated persons: particularly those operating within complex, multi-tiered supply chains who must achieve operational resilience and regulatory compliance across industries and jurisdictions. The Problem Compliance failures add costly administrative burdens and invite hidden vulnerabilities from their downstream data supply chain processors. Compliance processes require significant administrative effort which leads to increased chance of errors that can result in severe non-compliance penalties, failed inspections, undiscovered vulnerabilities in people, processes, software, data breaches, and ultimately lead to critical business disruption. The P3AUDIT Solution P3AUDIT reduces compliance-related administration by up to 80% and eliminates 100% of avoidable process errors. Using our proprietary circulatory technology, combined with AI and advanced automation, P3AUDIT delivers the following: > Capture, validate, and map compliance evidence for people, processes, and products > Ensure alignment with diverse industry and geographical regulations > Provide real-time visibility into an organization's overall compliance posture > Map data supply chains that include hardware, software and firmware sub-processors P3AUDIT gives clients the clarity and control they need to maintain uninterrupted business continuity—backed by verifiable compliance at every stage of their supply chain.
P3 LogiQ is an innovative software solution designed to streamline and automate the management of ISO and R2 compliance systems. By offering a complete, end-to-end platform, P3 LogiQ simplifies the complex processes of achieving and maintaining certifications. Our software helps businesses save time, reduce costs, and increase operational efficiency by automating compliance tracking, document management, risk mitigation, and employee training. With real-time reporting and continuous improvement tools, P3 LogiQ ensures your company stays audit-ready and aligned with industry standards, empowering you to focus on growth while we handle compliance.
Predict360 Internal Audit and Findings Management Software optimizes your audit procedures. Streamline audit workflows, capture all audit-related data in a centralized repository, and ensure timely collaboration. With features like audit plans, notifications, and integrated risk and compliance modules, you can efficiently manage findings and take corrective actions. Empower your business with a holistic audit management solution that provides clear visibility, reporting, and actionable insights.
Predict360 is an integrated risk and compliance management software platform for financial and insurance organizations. It integrates risk and compliance processes and industry best practices content into a single platform that streamlines regulatory compliance, improves efficiency, predicts risk, and provides best-in-class business intelligence reporting. Predict360 includes the following Risk Management applications: Enterprise Risk Management (ERM), Risk Management and Assessments, Risk Insights, Issues Management, Peer Insights, Third-Party Risk Management, Internal Audit and Findings Management, and Quarterly Certifications and Attestations. Predict360's Compliance applications are: Compliance Management, Compliance Monitoring & Testing, Complaints Management, Regulatory Change Management, Regulatory Examination and Findings Management, Policy & Procedure Management, Third-Party & FinTech Partner Compliance, and Marketing Ad Review.
ProcessGene GRC software solutions establish an automated workflow that reduces the time and cost of GRC efforts and eliminate manual labor, maintenance of multiple excel spreadsheets, etc.
Prodle AuditRoom is an An AI enabled unified audit workspace where auditors, suppliers, and stakeholders work seamlessly. Manage Documents • Meetings • Findings • Templates • Checklists • CAPA • Audit Reports , all in one workspace See Real results with : 50% faster audit turnaround time Remote audits for reduced costs & admin work AI tools for Improved audit accuracy Proactive detection of compliance gaps & risks Try it free: Contact sales@prodle.ai to schedule a demo or try the software
Generate Compliance Reports in minutes - not days. Qleer is the first AI platform built for Product Compliance & Certification Experts that automates product conformity assessment and radically accelerate tests report generation. Human centric, our platform moto is "Give your experts superpowers!". Qleer.ai does not replace human experts - it does the heavy lift cumbersome documentary and normative checks and deliver a draft report for review in minutes. The expert then makes final decisions.
QMex is a comprehensive, modular Quality Management Software (QMS) designed to help organizations digitize, standardize, and continuously improve their quality and compliance processes. Built specifically for regulated industries such as pharmaceuticals, medical devices, chemicals, and manufacturing, QMex enables companies to manage complex quality workflows efficiently while ensuring full compliance with international standards and regulatory requirements. QMex centralizes all quality-related processes on a single, integrated platform. Core modules include - Document Management, - BMR Printout, - Change Control, - CAPA (Corrective and Preventive Actions), - Deviation and Nonconformance Management, - Customer Complaint, - Artwork, - Out of Limit, - Training Management, - Risk Management (FMEA), - Supplier Qualification, - Audit Management, - and Annual Product Review (APR / PQR). This modular structure allows organizations to start with their immediate needs and scale the system as their quality maturity grows. QMex supports end-to-end traceability and real-time visibility across quality processes. Advanced reporting and dashboard features provide actionable insights, helping organizations identify trends, mitigate risks proactively, and drive data-driven decision-making. Role-based access control, electronic signatures, and audit trails ensure data integrity and compliance with GMP, ISO 9001, ISO 13485, and other relevant regulations. Designed as a secure, cloud-ready enterprise solution, QMex integrates seamlessly with existing ERP, LMS, and production systems, enabling organizations to create a connected digital quality ecosystem. Its user-friendly interface improves adoption across departments, from quality assurance and production to regulatory affairs and management. By replacing fragmented systems and manual processes, QMex reduces operational risk, increases efficiency, and supports a culture of continuous improvement. Organizations using QMex benefit from improved compliance readiness, reduced audit preparation time, and enhanced collaboration across teams—making QMex a strategic solution for companies aiming to modernize and future-proof their quality management systems.
We provide complete solution for Audit Management. This includes option for managing Internal Audits, Supplier Audits, 3rd Party Audits.
Qualifyze strengthens connections between manufacturers, suppliers, and global quality experts through digital solutions that enable smarter audits and proactive site risk management. Our platform combines a comprehensive audit library of 5,000+ ready to use audit reports, growing at a 40% annual rate, with centralized audit management, CAPA tracking, and site risk analytics to help healthcare and pharma companies manage quality and compliance across their supply chains in one place. Backed by 450+ quality experts, Qualifyze enables up to 65% faster audits and up to 50% cost savings by reusing existing audit insights, streamlining workflows, and providing early risk visibility to keep teams inspection ready.
QuantumByte Proof is an AI-powered evidence review layer for multi-location operations. It reads your standard operating procedures, checks every evidence submission your field teams upload — photos, checklists, corrective actions — and flags exactly where each submission falls short, across every location and every shift. Key capabilities: AI-assisted evidence review against your SOP across all locations; automated flagging of missed proofs, incomplete readings, and unclosed corrective actions; priority findings report with fix tasks assigned to the relevant location; compliance readiness score per location per shift; no change required to how your teams currently submit — Proof adds a review layer on top of existing workflows. Best-for/who it’s for: QuantumByte Proof is best for operations leaders who are responsible for standards across multiple locations, crews, franchisees, or service sites. Ideal users include: - Franchise directors and franchise operations teams - Directors of operations and VP operations - Regional managers and district managers - Brand standards and QA leaders - Field service operations leaders - Facilities and property management teams - Cleaning and janitorial operations teams - Restaurant, café, QSR, and foodservice operators - Gym, fitness studio, and wellness chain operators - Clinic and outpatient operations teams QuantumByte Proof is especially useful when your team already collects checklists or photos but still struggles to answer: “Did the work actually meet the standard?”