
Greater Compliance
Streamline compliance with FDA, EMA, ANVISA, WHO, avoiding audit deviations.

7x Faster
Reduce validation and qualification time by 7x with agile projects.

Lower Cost
Avoid rework and lower validation and qualification costs, fully paperless, in the cloud, enabling remote work.

Faster Time To Market
With no validation, biopharma and medical device industries cannot register or produce their products.
Streamline AI and traditional technologies validation
- All in one place
- Don't start your projects from scratch!
- Free 24/7 Training and Support
- Automatic Traceability Matrix
- Item-based approach
- Adaptable templates
- Empower teams
- Unlimited users
- Increase compliance

Reduce operations time by using a solution with strategic and integrated management.
Risk Management, Requirements Management, Test Execution, Incident Management, Inventory Management, Verification and Validation – V&V, Data Integrity, Access Control, Electronic Signature and more…

The only validation solution with qualitative content in the database.
The only one in the market with a library of risks, requirements, and tests available. Empower teams to independently carry out validations and qualifications and reduce external labor costs.

Ensure the success of your projects every step of the way. Study, train and prove your skills from anywhere.
Fast deployment process through training and exclusive attention, onboarding, access to the FIVE Academy, access to the Wiki (online tutorials), 24/7 support, standard functionality already validated, document kit for validation, support material and expert certificates included, and much more… Start validating from day one!

Automatically Generate Traceability Matrix, Save Time, and Increase Your Assertiveness.
Turn this deliverable into a management screen. Browse and manage your requirements and risk scenarios with just a few clicks.
Overcome the challenges of maintaining a validated state through an item-based approach.
It is not necessary to control a version of an entire document when carrying out the maintenance of a validated state or perform partial releases of systems, equipment, processes, and cleaning procedures.

Easy adaptable templates and processes.
Customize validation deliverables or work within well-established, ready-made templates.

Manage projects from anywhere in the world in real-time.
Healthier employees and more quality of life, online management, connecting teams across the world. Prioritize time on important actions.

Flexibility for profile assignment and user registration.
The access profiles can be freely configured by each client, and there is no limit to the number of users registered in the system; the licenses are for concurrent users (those accessing GO!FIVE® at the same time).
GO!FIVE® helps increase conformity by complying with FDA 21 CFR Part 11.
The data generated in GO!FIVE® is stored on a cloud server, with international certifications, which confirm the commitment to high levels of security, confidentiality, and availability of services.
Find out how quickly your investment in GO!FIVE® pays off and be surprised


Meet our clients
The Value We Generate
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GO!Startup Program
