CONTACT

True success is achieved through strategic clarity and operational precision, not through redundant effort. With the right expertise, you can eliminate inefficiencies, mitigate risks, and allocate resources only where they yield maximum impact. Our approach empowers you to distinguish priorities from distractions, aligning your efforts with initiatives that drive measurable outcomes. By optimizing processes, fortifying compliance, and enhancing organizational efficiency, we help you realize significant cost savings while strengthening long-term performance. Every decision becomes more purposeful, every action more effective. Partner with us to transform complexity into opportunity and ensure your investments deliver sustainable, high-value results.

RA QA Compliance

Please fill out the contact form and share as many details as you can, so we can fully understand and address your needs. If onsite services are required, please include your address, city, and country, as well as any relevant product details. We look forward to hearing from you and will make every effort to get back to you as quickly as possible. We are headquartered in San Francisco, California, and provide services worldwide. To better support our clients in Europe, the UK, and the rest of the Schengen Zone countries, we are available to travel directly to your location. When schedules allow, we strategically align visits with other companies in the region, enabling you to share travel expenses and significantly reduce costs. This flexible approach ensures you receive on-site expertise while maintaining efficiency and value. In addition, we are available to assist and advise during FDA inspections, whether remotely or on-site. However, due to scheduling demands, priority will be given to our existing clients.

Contact RAQA by ex-FDA Investigator

LOCATIONS

    • San Francisco, California, USA
    • Switzerland, the UK, Europe, and Schengen





    Partner With US

    For FDA expertise—whether in quality systems, regulatory compliance, CAPA management, mock FDA inspections, or responding to FDA Form 483 observations and warning letters—you have come to the right place. Our team consists of former FDA professionals who have been on the other side of the table and truly understand how inspections unfold. We bring firsthand knowledge, proven strategies, and practical insight to guide you through the complexities of FDA requirements. Our role is not merely to advise but to partner with you, offering clear guidance, actionable tips, and strategic support to help you anticipate, respond, and succeed in any FDA-related matter with confidence.