We are a global consulting organization for medical, biotechnology, and in vitro diagnostic device companies in ISO 13485 and CMDCAS registration preparation, ...

You are a provider of medical devices, in-vitro-diagnostics, active pharmaceutical ingredients, or a supplier to the pharmaceutical industry, or active in the ...

Willow River Consulting focus on Developing Quality Assurance Systems compliant to ISO 9001:2000, ISO 13485:2003, FDA 21 CFR 210, 211, and 820 (Pharmaceutical, ...

Smestad & Associates in San Francisco Bay Area (Palo Alto, California) provides regulatory and quality systems consulting for the medical device industry