Trusted by pharmaceutical leaders in 11 countries.
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.
Streamline AI and traditional technologies validation
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
Deborath Salamonczyk
I am very satisfied with the services provided.
Markieta Stevens
The team at FIVE demonstrated exceptional professionalism throughout this project. They were consistently encouraging, supportive, and highly effective in executing the validation activities to the highest standards. I look forward to collaborating with them on future projects. On behalf of the entire Galderma team, we sincerely appreciate FIVE’s guidance, commitment, and support throughout this engagement.
Murilo Knop
“I am very pleased with the quality and speed of service for open tickets in the Go!Five system. This effective and efficient support allows us to pass these qualities on to our operations and deliveries. Keep up the good work!”
Karina Souza
“I appreciate all the support and professionalism that went into delivering this project, which is so important to the company.”
Markieta Stevens
“I have enjoyed working with the team at FIVE and I am looking forward to future projects with this team.”
Victoria Miranda
“It is a company that has been validating the Omni system for years and has always delivered high-quality service. “
Maja Petinac
“I can say that GO!FIVE® is a very good solution for the validation process and that it makes work much easier. Almost everything the user needs is available and well structured.”
Simone Fernandes
“We express our satisfaction with the service provided, which fully met our expectations and requirements. We highlight the high technical quality and consistency of the risk analysis conducted throughout the work, demonstrating in-depth regulatory, methodological, and operational knowledge.”
Mayara Sá
“FIVE was essential in enabling us to conduct this validation satisfactorily. I would like to congratulate the team for their organization, clarity in the steps, and willingness to assist us with any questions we had. Without a doubt, it was a time of great exchange and learning, and I would recommend FIVE to any laboratory wishing to implement and validate a new system.”
Jéssica Alves
“The project was completed successfully and with commitment.”
Eliane Aguiar
“Excellence in service provided”
Fernando Alves
“Excellent work by FIVE, all the support provided was sensational! Everyone involved was patient, available, helpful, and objective. They clarified all doubts and suggested possibilities, always with justification and high-level technical knowledge.”
Helda Machado
FIVE presented a solid technical foundation, resulting in a robust and safe project.
João Mendes
The project was handled very well by Fagron’s validation team. We have always relied on FIVE’s expertize for our projects, which is why Fagron has been a FIVE partner for over 8 years. Here’s to the next projects!
Paôla Oliveira
I only took part in the project for a short time, in the final stages of the reports, but I was satisfied with the support provided and the guidance given. Meetings were agile and clear about the objective.
Luana Lemes
Exceptional service.
Agnes Morgana Gomes Candido
The project was delivered with quality, as expected, and the team’s service was always agile and helpful, promptly assisting with any doubts or problems. We were very satisfied with the partnership.
Murillo Henrique Araujo Eloy
I would like to express my special thanks to FIVE team for all the exchanges of experience and the challenges shared throughout this validation, which enabled us to finalize and prepare a consistent and well-structured document.
Bruno Dias Camargo
I liked the service provided, it was satisfactory and inclusive.
Pedro Miguel Cabrera Ruschel
FIVE employees have always been willing to do their work in the best possible way. I would like to thank FIVE team for their services.
Meet our programs
Partner Client
