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Innovative Medical Device Services | QA Consulting Your trusted medical device consulting and outsourcing partner for quality assurance, regulatory affairs, and microbiology analysis services throughout the product lifecycle
20 Years of Medical Device Experience | QA Consulting Lean into our quality and compliance know-how to bring your medical devices to market and beyond QA Consulting is your trusted partner for tailored quality systems, regulatory affairs, and microbiology analysis throughout the product lifecycle
Medical Device Post-Market Surveillance | QA Consulting, Inc. QA Consulting is here to help you plan, navigate, and implement all aspects of medical device PMS By leveraging the experience of an expert in post-market surveillance services, the process becomes thorough, painless, and risk-reduced
What Does Approved Supplier Status Mean? - QA Consulting, Inc. QA Consulting is on the approved supplier list for many leading multinational medical device companies, which is no small feat Approved suppliers must not only meet strict guidelines to gain approved supplier status but maintain those standards to ensure they stay on these lists
Meet Kathy Johnson - QA Consulting, Inc. We support rapport-building by regularly spotlighting our team members so you get to know the people behind QA Consulting Meet Kathy Johnson, Human Factors and Usability Engineering Consultant Get to Know the Experts — Five Questions with Kathy
How to Avoid Dose Audit Failures and What to Do When It Happens to You QA Consulting is the medical device consulting partner you need with the knowledge and experience to apply to your unique device For more in-depth information and guidance on managing sterility failures, explore our detailed white paper on the topic and set up a discovery call today
Client Testimonial: From R D to Compliance With Efficiency Solution: QA Consulting, Inc developed standard operating procedures (SOPs), wrote and executed software validation protocols, and provided flexible document control support Outcome: QA Consulting provided an FDA ISO compliant QMS and the structure our R D team needed to create design history files (DHF) for submission to regulatory bodies
Medical Device Document Control | QA Consulting, Inc. The QA Consulting team are experts in EU market access and MDR pre- and post-market regulatory processes Learn from our years of experience and let our personalized approach bridge the gap in your current QMS document control
Design Controls for Medical Device Manufacturers - QA Consulting, Inc. Connect with QA Consulting Having helped hundreds of medical device companies accelerate product development, remain compliant with regulatory guidelines, and mitigate risk at each stage of the product lifecycle, our experts are ready to help your team