Advantu is the leading nationwide Software Quality Assurance/Testing, Software Engineering, SDLC Process Improvement & FDA Regulatory Guidance & Support Firm. We help R&D Teams increase productivity, shrink time-to-market and improve customer satisfaction with their products. Medical Device Manufacturers utilize Advantu's 30 years of Biotech experience to improve Patient Safety for their customers, while benefiting from our Regulatory experience to ensure successful FDA submittals (for the new products in their pipeline), and ensuring their Quality Management System is accurate and complete. Additionally, Pharmaceutical companies have benefited from our expertise via Gap Analysis of their entire QMS, in order to improve R&D/Manufacturing/Supplier Quality and CAPA issue reduction. With their Manufacturing Processes properly aligned with Good Manufacturing Practices (GMP), our clients have reduced line losses and delays, while dramatically decreasing Time to Market for their products. Advantu's proven Risk ID process ensures our clients can prevent product recalls and measurably improve product quality and reliability across their portfolio. This program provides the (value-added) benefit of a high degree of confidence at product release. Headquartered in San Diego, Advantu is privately held by its executive team and is well positioned to support your Medical Device & Pharmaceutical Project across the continent. For content, updates, newsletters and more: http://advantu.com/category/news-blog/