Leading Alternatives to Digital Quality Management Suite for Your Business

CAQ software from Babtec: all tools for quality management in one solution.

Greenlight Guru is a modern and comprehensive system that allows medical technology companies to manage the entire lifecycle of their product in one place with Part 11 compliant e-signatures and flexible review & approval workflows. It offers powerful design control objects, document attachments, integrated quality and risk management, Nonconformances, Audits and CAPAs control, and communication across applications. This eliminates the need for unnecessary meetings or emails, saving time and effort while staying compliant and up-to-date with the most current version.

E-Data Now! is an Audit and Quality Inspection platform used to improve processes and grow customer satisfaction. Collect data in real-time and track team inspection processes in remote locations using mobile devices. The powerful inspection tools used to record the inspection data with compliance and triggers corrective action. Get real-time reporting and trends on your performance dashboard.

Enzyme is a quality management system and a regulatory submission platform that provides companies with the complete solutions that they need. The software includes modules for all stages of the product development life cycle from Design Control to CAPA. Enzyme’s QMS includes modules that cover the key components of 21 CFR 820 and ISO 13485. The software features design control, document control, training, complaints, audits, suppliers, Nonconformance and corrective & preventive action, accordingly. Enzyme’s QMS is designed for use in a modern, agile software development process. One can import existing data into Enzyme so they don’t have to repeat the work. Furthermore, one can generate reports directly from Enzyme which can be used for submission. Enzyme's objective is to enable life sciences organisations to develop more effectively and quickly. The platform supports the development and commercialisation of digital, drug-device combination, diagnostic, software/hardware, and disposable healthcare products. The platform guarantees that a product is properly verified and validated prior to design transfer and submission, lowering the risk of rework and project churn.