Inspection-Ready, Phase-Appropriate QA Systems for Pharmaceutical, Biotech, CDMO, and Advanced Therapy Companies
Altabrisa Group supports life sciences companies in building and optimizing quality assurance systems that withstand regulatory scrutiny and enable operational growth. We help teams design, implement, and remediate QA programs aligned with FDA, EMA, ICH, and WHO expectations.
From early-phase design to post-inspection remediation, Altabrisa Group delivers strategic, scalable QA support that meets the expectations of FDA and global regulators.
Altabrisa Group Limited, LLC
1309 Coffeen Ave, Suite 832, Sheridan, WY 82801
📞 Raleigh Office: 919-297-2800
📧 Email: info@altabrisagroup.com
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Our team of seasoned subject matter experts, each with over 20 years of experience, provide tailored solutions for organizations of all sizes. At the core of our services is our proprietary AdaptiStrat® System, a cutting-edge approach designed to deliver lasting results and drive quality. By combining our consultants’ wealth of expertise with this innovative system, we are uniquely positioned to help clients achieve their goals and create a solid foundation for compliance and regulatory success.
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Are you looking to improve your quality standards and ensure compliance in pharmaceuticals, biotechnology, vaccines, and cell and gene therapy industries?
Contact us today and schedule a free initial consultation with the experts at Altabrisa Group.
We offer personalized advice and strategies to help you develop, implement, and optimize your cGMP quality systems, ensuring your products meet the highest standards of safety and effectiveness.
Reach out to us today and take the first step towards excellence in quality and compliance.
Quality Excellence Powered by Strategic Solutions
cGMP & FDA Compliance Consulting for Pharma, Biotech, Cell & Gene Therapy, Vaccines, CDMOs, and GMP Labs
📍 Sheridan, Wyoming Office
📞 +1-307-461-5690
📍 Raleigh, NC Office
📞 +1-919-297-2800
📧 Email: Info@AltabrisaGroup.com
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