Your quality processes.
Made collaborative.

Work in real-time with your team on your quality processes, all in one place. Gain real-time visibility, faster decision-making and improved outcomes.

Unify your processes, enhance collaboration, and accelerate decision-making with Unifize—built for ISO and FDA-regulated companies.

MODERN, COLLABORATIVE, AND FLEXIBILE EQMS

Are you fed up with your clunky quality system?

Unifize's unique approach to collaboration brings people, processes and data together in a familiar, easy-to-use chat based environment.

Why Unifize?

A single source of truth for people, processes, and information

Watch on to learn how Unifize unifies fragmented systems and help reduce risk, boost productivity, and accelerate time to market. 

Industries

Here’s how effortlessly Unifize adapts to the unique requirements of your industry

Delivering tailored solutions that enhance collaboration and streamline processes for all industries.

Unifize optimizes quality management with streamlined document control, risk mitigation, and industry-standard compliance, driving operational efficiency and product integrity.
All
View Process Map
CAPAs and NCs
Identify, document, and resolve non-conformities; implement corrective/preventive actions.
HOW IT WORKS
Electronic Batch Records
Capture critical batch info such as materials used, manufacturing steps, calibration, QC tests, batch releases.
HOW IT WORKS
Training
Track and ensure employee training on procedures, regulations, and device handling.
HOW IT WORKS
Document Management
Control, track and manage documents required for compliance with FDA Part 820 and ISO 13485.
HOW IT WORKS
Unifize optimizes automotive quality management with streamlined design control, supplier collaboration, and compliance, driving excellence in product quality and safety.
Automotive
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Document Management
Control, track and manage documents required for compliance with IATF 16949, ISO 9001
HOW IT WORKS
APQP (Advanced Product Quality Planning)
Streamline your development process with APQP for enhanced product planning, risk assessment, and process control.
HOW IT WORKS
PPAP
Manage your production part approval process (PPAP) with our software for seamless documentation, validation, and supplier collaboration."
HOW IT WORKS
FMEA
Identify and discuss failure modes, causes, effects, severity, detection, risk priorities of your product, design & process
HOW IT WORKS
An eQMS purpose-built for medical device companies. Unifize streamlines your medical device product development while keeping your teams compliant.
Medical Devices
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Revision Control
Ensure devices meet predefined specifications, with proper documentation, review, and approval of changes & revisions by the right people.
HOW IT WORKS
Training
Track and ensure employee training on procedures, regulations, and device handling.
HOW IT WORKS
Document Management
Control, track and manage documents required for compliance with FDA Part 820 and ISO 13485.
HOW IT WORKS
Design Master Record
Manage device specifications, manufacturing processes, labelling, packaging and quality control procedures.
HOW IT WORKS
Unifize optimizes manufacturing quality management with streamlined document control, risk mitigation, and industry-standard compliance, driving operational efficiency and product integrity.
Manufacturing
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Document Management
Control, track and manage documents required for compliance with ISO 9001 & ISO 14001
HOW IT WORKS
Training
Ensure employees are trained on safety practices and quality procedures, including when controlled docs are revised.
HOW IT WORKS
Product & Raw Material Specifications
Collaborate on drawings, work instructions, material & process specs, test specs, regulatory requirements and other docs
HOW IT WORKS
Revision Control
Ensure all docs and specs have proper documentation, review, and approval of changes & revisions by the right people.
HOW IT WORKS
Unifize revolutionizes nutraceutical quality management with seamless audits, complaint tracking, and robust supplier quality management, ensuring compliance and superior product standards.
Nutritional Supplements
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Product & Raw Material Specifications
Collaborate and manage product and RM specifications, including labels/artwork, allergens, storage, packaging etc.
HOW IT WORKS
Document Management
Control, track and manage documents required for compliance with SQF, BRC & 21 CFR Part 111
HOW IT WORKS
Training
Ensure employees are trained on safety practices and quality procedures, including when controlled docs are revised.
HOW IT WORKS
Recipe & Formulation Management
Manage recipes, formulations, and ingredient specifications to ensure consistency and compliance with regulatory requirements.
HOW IT WORKS
Unifize elevates aerospace quality management through streamlined design verification, configuration control, and maintenance tracking, ensuring regulatory compliance and exceptional product quality.
Aerospace & Defence
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Product & Raw Material Specifications
Collaborate on drawings, work instructions, material & process specs, test specs, regulatory requirements and other docs
HOW IT WORKS
Training
Ensure employees are trained on safety practices and quality procedures, including when controlled docs are revised.
HOW IT WORKS
Document Management
Control, track and manage documents required for compliance with AS 9100, 9110, 9120, ISO 9001
HOW IT WORKS
ITAR Compliance
Ensure all ITAR controlled docs & data are stored in compliant locations and retrieved only by authorised individuals.
HOW IT WORKS
Unifize ensures food safety compliance by streamlining HACCP implementation, supplier management, and audits, guaranteeing top-quality products and regulatory adherence.
Food Production
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Product & Raw Material Specifications
Collaborate and manage product and RM specifications, including labels/artwork, allergens, storage, packaging etc.
HOW IT WORKS
Document Management
Control, track and manage documents required for compliance with SQF, BRC & CFR Part 111
HOW IT WORKS
Training
Ensure employees are trained on food safety practices and quality procedures, including when controlled docs are revised.
HOW IT WORKS
Recipe & Formulation Management
Manage recipes, formulations, and ingredient specifications to ensure consistency and compliance with regulatory requirements.
HOW IT WORKS
Unifize empowers cosmetics companies with effective quality management, including streamlined audits, complaint handling, document control, and supplier management for compliant and safe products.
Cosmetics
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Document Management
Centralized storage, version control, and automated workflows to comply with 21 CFR Part 700, EU Cosmetics Regulation (EC No 1223/2009) and ISO 22716.
HOW IT WORKS
Electronic Batch Records
Digitally control batch releases, record batch production data, ensuring traceability and adherence to product & raw material sepcifications.
HOW IT WORKS
Recipe & Formulation Management
Manage formulations, and ingredient specifications to ensure consistency and compliance with regulatory requirements.
HOW IT WORKS
Product & Raw Material Specifications
Collaborate and manage product and RM specifications, including labels/artwork, allergens, storage, packaging etc.
HOW IT WORKS
Unifize simplifies quality management for CROs with compliant document control, streamlined audits, and seamless collaboration, ensuring successful research and development projects.
Contract Research
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Document Management
Streamline document management and compliance with GLP, GCP, ISO 17025, GMP, HIPAA, ICH, and CFR.
HOW IT WORKS
Method Validation and Verification
Manage the validation and verification of test methods, ensuring compliance with ISO/IEC 17025 requirements.
HOW IT WORKS
Sample Storage and Tracking
Manage sample storage and track sample locations, ensuring proper organization and easy retrieval.
HOW IT WORKS
Test Method Management
Centralize and manage test methods, ensuring version control, accessibility, and compliance with standards.
HOW IT WORKS
Unifize enhances laboratory quality management with streamlined audits, document control, and compliance, ensuring accurate and reliable results through effective collaboration.
Laboratories
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Document Management
Simplify ISO 17025 compliance with robust document management capabilities, ensuring traceability, version control, and easy access to critical records
HOW IT WORKS
Test Method Management
Centralize and manage test methods, ensuring version control, accessibility, and compliance with standards.
HOW IT WORKS
Sample Storage and Tracking
Manage sample storage and track sample locations, ensuring proper organization and easy retrieval.
HOW IT WORKS
Method Validation and Verification
Manage the validation and verification of test methods, ensuring compliance with ISO/IEC 17025 requirements.
HOW IT WORKS
A quote from Denis Machoka
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Denis's experience with Unifize: Revolutionizing quality assurance systems

Quality expert Denis details his transformative journey with Unifize. He praises its efficient design, user-centric approach, and the system's ability to streamline data handling and accelerate time to market.

A quote from Clarissa Archer
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Harmonic Bionics and Unifize: A seamless transition to regulatory compliance

Clarissa Archer shares her experience integrating Unifize into Harmonic Bionics, underscoring its value in streamlining change control, facilitating communication, and ensuring robust documentation for regulatory compliance in the medical device sector.

A quote from Michael Hogan
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Engineering efficiency with Unifize: Michael Hogan's insights from Harmonic Bionics

Mechanical Engineer Michael Hogan elaborates on how the integration of Unifize at Harmonic Bionics has streamlined his engineering processes, promoting transparency and rapid turnaround in the medical device domain.

A quote from Jesse Kolstad
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Here’s how Biovation Labs reduced testing costs from $146K to $65K in two months

Learn how and why Biovation Labs, an FDA regulated nutraceutical manufacturer based in Salt Lake City, took the decision to transition from MasterControl to Unifize for their product lifecycle (PLM) and quality management (QMS) processes.

A quote from Tedd Carr
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How a quality veteran from boosted issue closure time by 75% within the first month

Tedd Carr from The Will-Burt Company discusses overcoming their diverse and complex quality challenges across various sectors with Unifize. By consolidating five systems into one, they achieved clear accountability and reduced issue closure from months to days, demonstrating significant efficiency gains and faster decision-making in their quality processes.

Testimonials

And here’s what

our customers are saying

We didn’t reinvent the wheel, just quality management

Transform your operations with tangible benefits.

Benefits

Slash time-to-market by 70%
Map Unifize to your processes and streamline workflows, process automation, and prioritization.
Reduce meetings by 90%
Less meetings with in-app collaboration, real-time updates, and decision logs.
Improve accountability by 2x
Drive accountability using task assignments, deadline reminders, and progress tracking.
100% Visibility
Full visibility through real-time reporting, milestone tracking, and customizable analytics.
Eliminate 100% of internal silos
Reduce internal silos with unified communication channels, team chats, and project dashboards.
“The platform has given us the opportunity to be 100% transparent with each other and allowed for collaborative efforts to ensure all processes are aligned, streamlined, and effective.”

Integrations

Curious to unify your other systems with our platform?

Click below to speak with sales.

Book a Demo
Witness Unifize’s collaboration-first approach to solving quality challenges
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