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Arbour Group offers validation and compliance services for the pharmaceutical industry, ensuring the quality and safety of products while following US Food and Drug Administration (FDA) and international regulatory guidance.
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Medical Devices

Arbour Group assists medical device companies with compliance related to the requirements of the FDA and other international regulatory agencies as well as the guidelines contained in ISO 13485, Quality Management Systems, ISO 14971 and Application of Risk Management to Medical Devices. We help clients achieve a culture of compliance that raises quality levels, reduces risk and costs as well as increase shareholder value.

Arbour Group provides assistance to Biotechnology companies related to managing the risk associated with the development and manufacture of drugs, vaccines and antitoxins. We can provide the industry experience and expertise necessary to assure that risk is appropriately addressed and the procedures and controls are in place that will assure compliance.

The Diagnostics segment of the life sciences industry is one of the fastest growing. Companies in this segment develop the reagents, instruments and systems that are intended to diagnose disease as well as disease mitigation, treatment or prevention.