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2016 FDA Regulatory Symposium for Medical Device Industry

Conference to discuss FDA 2016 trends, Impacts of 483s, warning letters and legal actions within domestic and international markets in the medical devices industries.  We will discussed the FDA Compliance programs, among other relevant topics.

2016 Fda Regulatory Symposium For Medical Device Industry


Ms. Teresa Jimenez – Over 25+ years of experience Internationally Medical Device Consultant with a strong record of accomplishments in FDA regulatory affairs and quality assurance. Former FDA Medical Device National Expert with vast experience in quality systems and Good Manufacturing Practices for the medical device industry.

Mrs. Yanira Torrellas – Over 15+ years of experience in the Medical Device, Pharmaceutical and Biotechnology Industry with vast expertise in Compliance Remediation Plans. President of Quality Consulting Group; company recognized by PharmaTech Outlook as One of the Top Ten Pharmaceutical Solutions Provider.

Course Details:
Date: Wednesday November 2 2016
Duration:  8:00am – 5:00pm
Location: Real InterContinental, San José, Costa Rica
Price: $525.00 FDA SYMP  –  $625.00 FDA SYMP + Cocktail

Contact us if you have any questions: (787) 418-0240

Click Here For More Information and Register!

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