Altabrisa Group LLC is a dynamic U.S. based Pharmaceutical, Medical Device, and Biotechnology Consulting Firm with offices in both United States and Mexico. We provide exceptional GXP (GCP, GLP and GMP) consulting services to clients in the United States, Latin America, Europe, and Asia. Our goal is Tailored Approach and Global Delivery.
While we specialize in Quality Systems and Remediation (483 and Warning Letter responses), and Data Integrity, our extensive consulting capabilities allow Altabrisa Group to assist you in meeting your quality, regulatory, laboratory, manufacturing, and validation needs.
Altabrisa Group Limited has worked with many of the world’s leading pharmaceutical, biotech and contract management organizations, including start-ups. We are uniquely positioned to serve life sciences, biologics, biotech, and medical device organizations of all sizes.
If you need assistance with FDA Responses, Quality Remediation, Data Integrity Assessments, or just a typical audit, look no further and give us a call. We understand your business. Our proven techniques and methods have resulted in long-term, sustainable results for many organizations.
Our Tailored Approach to your unique problem means that you get compliance focused, cost effective results.
Our associates have over 20 years of industry experience and come from some of the best companies in the United States. Additionally, each consultant has Tier I consulting experience. That means you get top quality consultants without paying top of the range consulting rates.