Comprehensive GMP & Compliance Consulting Services

Strategic, technical, and operational consulting support for life sciences companies regulated by the FDA and global agencies.

Your Partner for Quality, Compliance & Inspection Readiness

Altabrisa Group delivers specialized consulting services that help pharmaceutical, biotech, CDMO/CMO, vaccine, cell therapy, and GMP laboratory organizations build and sustain compliance with FDA, ICH, and global regulatory requirements. From QA/QC to deviation management and inspection preparation, our consulting services are built for real-world execution.

Consulting Services

Quality Control Consulting

Quality Assurance Consulting

Data Integrity Consulting

Quality Audits

Deviation Management Consulting

Quality Systems Consulting

Batch Record Review

Document Management

Training, Coaching & Mentoring

CAPA Management

Change Control

Person-in-Plant Oversight

FDA Readiness & Mock Inspections

Lean QC Laboratory

Retrospective Deviation Review

3rd Party Batch Record Certification

FDA Regulatory Response

Schedule Your Free Initial Consultation

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Built for Compliance. Powered by Strategy.

Get Expert Help Today

Ready to reduce risk, improve compliance, and close the gaps in your quality systems? Connect with Altabrisa Group for a no-cost discovery call.

Altabrisa Group Limited, LLC
1309 Coffeen Ave, Suite 832, Sheridan, WY 82801
📞 Raleigh Office: 919-297-2800
📧 Email: info@altabrisagroup.com

Pricing

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Schedule Your Free Consultation Today

Partner with Altabrisa Group and leverage our expertise to improve, simplify, and streamline your quality compliance. 

Contact us now to build a partnership that achieves a strategic compliance solution that meets your unique needs. 

Let’s build quality together!