Date :
Place : United States, San francisco
Contact Person:Paula Edwards
Description:
It has only been a few years since the FDA released its guidelines for human factors and usability testing for combination products. Compared to medical device companies, dedicated pharma and biotech companies have had to cope with a very high learning curve in order to meet regulatory expectations. For lack of long-term experience on this subject, many companies continue to struggle to build the necessary human factors expertise, whether through outsourcing or intensive team training.Deadline for abstracts/proposals : 12th February 2018
Organized By :New York Events List
Keynote Speakers :
Conference Highlights :Updates on the latest regulatory developments, including how to proceed when CDER and CDRH reviewers seem to disagree Best practice for sequencing validation studies within the product testing life cycle to avoid severe late-stage errors Device instruction and labeling optimization strategies that reduce user error
Venue :San Francisco, CA, United States
Check the event website for more details.