Best Practices

➣ Easily customized and pre-configured processes.

➣ Efficiently meets and exceeds industry demands, standards,

 and compliance requirements.


➣ Agile and cost-effective customization.

➣ Full API and integration

➣Scalable for organizations of all growth stages and sizes.


➣ High Availability

➣ Disaster Recovery and backup.

➣ ISO 27001 Security certification

➣ Scalable

➣ Trusted and tested Platform

Cost Effective

➣ No capital investment Required.

➣ Competitive pricing for optimal value.

➣ Minimal IT costs.

User Experience

➣ Intuitive, user-friendly interface: minimal learning curve, maximized adoption.

➣ Smooth & simple navigation.

➣ Customizable UI features and options.

➣Consistent and streamlined.


➣ Mobile enabled: ideal for smart devices & tablets.

➣ iOS and Android apps available.

➣ Consistent, reliable cross-platform performance.

Ecosystem Support

➣ Secure portal access for suppliers & external labs.

➣Powers easy view and updates of relevant data.


➣ Built-in flexible reporting for measurable insights.

➣ KPI’s and scorecards to optimize productivity and performance.

➣ Easy data export for metrics and stats.

What We Do

Latest News & Updates


Come and meet us at MEDICA fair on 12 - 15 November 2018, Düsseldorf / Germany. Hall 8b / L33 (Compamed).

Contact us in order to schedule a meeting!

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Industry Standards

ISO 13485

Dot Compliance Suite is designed to support key features required by ISO 13485, such as document/record control, control of design and development changes, supplier evaluation and selection, complaint handling, audits, CAPA (Corrective and Preventive Action), device history record and training.


Dot Compliance Suite is developed to offer the ideal set of features necessary to ensure quality food manufacturing practices, such as change control, deviation handling, document/record control, supplier evaluation and selection, complaint handling, audits, CAPA (Corrective and Preventive Action) and training.

FDA 21 CFR Part 11

Dot Compliance Suite’s technology provides the foundation for a centralized system offering key modules and features required by the FDA to manage electronic records, as our solutions including full audit trail and traceability, electronic signatures, and a validation package.