ISO Telephone Seminars

PDS PIPING TRAINING BIBRAIN WITH OFFER CHENNAI Good day and thank you for the interest on our course. "LEARN THE BEST FROM THE PIONEERS - PDS, SMARTPLANT 3D - THE REVOLUTIONARY NEXT GEN 3D SOFTWARE ONLY @ BIBRAIN INSTITUTE (ISO 9001: 2008 CERTIFIED) PDS, PIPING, CADWORX AVAIL EXCLUSIVE OFFERS! Pay for PDS course and learn other software free of cost. Limited period offer. Fresh Batch starts NEXT WEEK. Register for your seats  more...

Purchasing and Supplier Controls in the Medical Device Industry - Webinars GlobalCompliancePanel This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices. Wednesday, November 16, 2011 10: 00 AM PST | 01: 00 PM EST  more...

Supplier Evaluation and Assessment How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar By Global This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. Supplier qualification and assessment is required in both the QSR regulations and ISO standards.  more...

Understanding Analytical Test Results Comparing Two Sets of Data - Webinar by GlobalCompliancePanel The class will cover the understanding the properties of single test results and how they may be compared. There are many problems that arise from a misunderstanding of the properties of single data sets and the problems are compounded when data sets are compared. The discussion will cover the misconceptions and present methods to allow proper comparisons, while considering the risks inherent  more...

Device Changes FDA Changes and the 510k - Webinar by GlobalCompliancePanel The majority of medical devices are cleared for marketing in the U. S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when one change is major enough to impact safety / effectiveness, or when a series of lesser changes finally reach the "tipping point". This is a major headache. How can companies make that determination? How can they trigger such  more...