Arbour Group L.L.C. is a global leader specializing in providing a full scope of regulatory products and services for computer systems and medical devices within pharmaceutical, medical device, and biotechnology companies worldwide. As regulatory compliance specialists, our expertise is in designing, integrating, supporting, and validating critical software applications. Arbour Group's regulatory products include packaged validation protocols that help clients ensure that key ERP solutions are functional and in compliance with applicable regulations to minimize business risk. Our regulatory services are based on a results-oriented software testing process that not only assures compliance and functionality, but also responds competitively to the needs of customers by ensuring product quality and reliability.
To help clients ensure that key business systems are functional and in compliance with applicable regulations, our professionals have the technical qualifications, the management foresight, and the international support systems to address critical issues for clients in managing their firms' global business risk. Headquartered in Chicago, Arbour Group also has offices in California and New Jersey, and is supported by international centers in Dubai, U.A.E., and Dublin, Ireland.
ARBOUR ADVANTAGE
As a premiere provider of regulatory compliance and software testing services, Arbour Group offers you the convenience and economy of one-stop shopping for all your compliance needs. A number of clients rely on our comprehensive capabilities to outsource their entire testing process. From a broad-based project orientation to a focus on a particular software package, our regulatory compliance and software testing specialists are at your service. We have the ability to work with your purchased software applications, as well as with software you may have developed in-house.
We also have the flexibility to perform our regulatory compliance and software testing services at your site or at our Global Test Center. Here is a list of some of our regulatory compliance and software testing advantages:
- Life Sciences Focus
- Innovative Products to Reduce Costs
- Time Proven and Agency Weathered Methodologies- Reduce Risk
- Results-Oriented and Client Tailored Approach to Streamline Project Tasks
- A Global Presence Allows Harmonization of Regulatory Compliance Across Diverse Software Systems, Dispersed Facilities and Complex Regulatory Environments
- Warranted Deliverable
OUR MISSION is to develop and deliver regulatory compliance products and services along with the convenience and economy of one-stop shopping for all validation and testing needs.
OUR CLIENTS rely on our comprehensive capabilities to outsource their entire validation and testing processes.
OUR REPUTATION as "Regulatory Compliance Specialists to the Pharmaceutical and Medical Device Industries" is built on an ability to provide premium quality products and services at every level of delivery.
What we do for you:
- Ensure accountability and facilitate regulatory compliance
- Help ensure that electronic records and signatures are in compliance with 21 CFR Part 11
- Implement procedures to maximize operating efficiencies
- Effectively manage the cost of regulatory compliance
- Assist clients in responding to the full scope of requirements imposed by the Sarbanes-Oxley Act
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