Allegiance Regulatory Consulting LLC

Allegiance Regulatory Consulting provides regulatory services to support our clients’ needs for product registration and compliant product development to allow them to launch and sell their products globally.  We help clients navigate through the medical device regulatory maze throughout the product development life cycle, from providing regulatory strategies to ensuring compliant systems and documentation.  With our understanding of the perspectives of both the regulatory reviewer and the product engineer/designer, we document and submit product registration applications for our clients to regulatory authorities, like the FDA, Health Canada and EU notified bodies.  We can also provide training to educate employees on regulations to ensure efficient and timely product launches.

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