From start to finish, our Sales then Implementation Engineer, and customer Success Rep have been A.

Overall the ARENA PLM System is very user friendly and a very powerful tool.

My experience with Arena has been fantastic so far. They aim to please and are improving the product all the time.

With so many assignments and tasks it is hard to keep track of them.

I am very impressed with Arena, it seems to be designed by people that understand Product Life Cycle Management, Quality Systems, Regulatory compliance.

Our ECO turn around time decreased, we were able to make changes to parts and various BOMs quicker and easier.

I like that I can search whatever product I need to understand and see all documentation tied to it. I also enjoy the traceability of said documentation for doing investigations for failure analysis.

It was difficult to get ahold of customer service and the communication coming from the Arena team was unclear. They were so difficult to work with.

There is no out of office function to pause training due dates for employees with an extended out of office.

Fully Customizable eQMS with great support and pricing.

Ability to compare BOM differences. Easy to track engineering changes/revisions.

As a person who has never used Arena, it was very easy to use and navigate with little training.

The BOM and Part system are great. It is easy to do ECOs and have Arena integrate with ERP systems such as SAP.

I have used MasterControl and when I have to change training due dates in Arena, there is no option to include a comment when I have to change a user's training due date.

There are a couple of feature enhancements that I've been waiting for a while now, but I also recognize that. There are workarounds for those missing elements that are functional, just not pretty and.

Great PLM and BOM system that integrates well.

Overall the software has been very useful to our company and the customer service has been outstanding.

ARENA is a very user friendly platform and easy to navigate.

The change module, items module, and quality module, ease of use, and customer service at ARENA.

Quality module is the most like function what i used. Like the nonconforming material control connect with CAPA, and easily to update the layout.

A team that no longer is with the company made a number of decisions that ended up causing a lot of trouble (for me specifically, as the admin/quality rep) in the future.

The ease with which you find all the documents and the way of navigating.

Greenlight Guru is a Great Document and Project Management Suite.

Document Management is weak when it comes to controlling revisions when updating or revising a document.

Guru has allowed us to, from a very young, inexperienced stage, build from scratch an easy to use and comprehensive quality system that has passed external audit with ease.

QMS software is very easy to use and get around with.

Hope to see GL grow, because their customer service is A+ and their advice and consultancy calls are also really good.

This is useless if you don´t know the right name of what you are looking for. Second deficit:  We were told that data exchange with other systems is not possible.

Ease of use and very intuitive interface. Navigating the platform is very easy and functions such as uploading documents and routing are very easy to use.

The software itself is essential for any small-medium company hoping to get through the product development process and receive FDA clearance/approval.

Document management is very easy to use and provides for easy review. There are many updates to the software so the service is always improving.

And I must commend their customer support team - they are an admirably responsive and helpful team of people who add so much value to the experience with this company.

Easy to use and learn, integrates the entire Quality Management System into one interface.

The ability to properly and effectively manage our quality system and eliminate all paper documents.

Its an excellent tool with very good customer support.

I think the menus are a little slow and confusing though.

I love how you can link tasks, documents, investigations, and CAPAs.

The team at Greenlight is extremely passionate and have been amazing at supporting us and answering questions in record time.

Sleek Medical Device QMS Software with a great Team.

The design and development module is truly the reason we purchased Greenlight. It is extremely simple, allows for easy/agile development and review and integrates risk.

It changed the way we documented risk related to the products.

It's very hard for QMS software to be friendly and this one is super friendly all the time. Software has some of the remarkable QMS solutions for the medical device industry.

Very impressed by the software platform. Highly recommend medtech companies leverage this software platform to improve overall productivity.

The customer support, user interface, and turnkey solution offered by Greenlight. Guru has exceptionally useful for us, and  been the foundation for Quality Management at our company.

Users who were in the application at the time of document routing received no notification a document was waiting for them.

Overall experience is great. As a small medical device company, I can't imagine keeping up with our QMS requirements without a software platform like Greenlight Guru.

We are saving a lot of time because it is so easy to link data to each other, and hence have the desired traceability.

I personally love their DMS and Customer Feedback workflows. They're easy on the eyes, tell the whole story and allow for easy routing and approving to key stakeholders.

To date, GG has been an excellent partner in the implementation of an otherwise difficult system.

The system doesn't have an efficient way to implement P1xP2 analysis of risk probability, and is harm-centric.

Customer service is quick to respond and Greenlight Guru is always taking suggestions for improvement, they have even implemented some.

We didn't need to hire a quality manager because of how helpful this software is, a fact that alone makes it worth the price.

US Dollar

Arena helps innovative electronic high-tech and medical device companies of all sizes create products that change the world. Arena unifies product lifecycle (PLM) and quality management (QMS) processes, allowing every participant throughout the product realization process, from design to manufacturing to working together. With Arena, teams accelerate product development and delivery to increase profits. 

Arena's product-centric QMS solution streamlines product realization processes with links to relational bills of materials (BOMs), engineering changes, and quality records to eliminate disconnected silos. Arena’s comprehensive quality management system improves the management of Standard Operating Procedures (SOPs), Device Master Records (DMRs), and Design History Files (DHFs) to simplify compliance and reduce audit risks. 

With their deep product knowledge and specific industry expertise, Arena solutions consultants are knowledgeable enough to enable companies to be successful from first implementation to further expansions. We will guide you through configuring our solution to meet your unique needs and are always available to assist with any issues you may experience. 

LongDescription

ISO Standards Management

Document Storage

Access Controls/Permissions

Change Management

Complaint Management

Risk Management

Audit Trail

Compliance Management

Real Time Data

Training Management

Issue Management

Document Coding & Control

Defect Tracking

Activity Dashboard

Quality Control

Document Review

Audit Management

Supplier Quality Control

Monitoring

Supplier Management

Incident Management

Corrective and Preventive Actions (CAPA)

Third-Party Integrations

Document Management

Quality Assurance

Compliance Tracking

Workflow Management

Reporting & Statistics

Version Control

Customizable Reports

Approval Process Control

Data Import/Export

Alerts/Notifications

Customizable Templates

Task Management

Email/Help Desk

Knowledge Base

Phone Support

Chat

2-10

11-50

51-200

201-500

501-1000

1000+

Arena QMS

In Person

Live Online

Webinars

Documentation

GreenlightGuru is a cloud-based quality management solution designed specifically for the medical device industry. It provides premarket and post-market solutions which are Greenlight Go and Greenlight Grow. Key features include design control, risk management, audit management, complaint management, change management and training management.


Greenlight Go features design control that lets users maintain traceability. Users can create design control objects and attach documents with them. The solution offers auto document routing and revision control as well. Additionally, Greenlight Go allows users to view relationship between requirements, risks and verification tests.


Greenlight Grow features CAPA management that identifies and addresses the issues. Audit management allows users to manage tasks, follow-ups, communications and actions relating to audit findings. Final audit summaries can be created and shared. With nonconformance management, users can capture defect details such as part, quantity, failure type and severity.


Support is provided via phone, email, live chat, online training, podcasts and online documents.



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