Training Best Practices for Life Science CompaniesUse this four-step process to build a system that meets regulatory requirements
Tue, 02/24/2015 - 13:58
No matter how good your written policies are, or how clean a facility you operate, or how successful you are in the marketplace, it can all fall apart without a strong handle on your organization’s training needs and ability to effectively manage a… Are You Ready for 21st-Century eMDR Submissions?The rules are changing
Tue, 12/09/2014 - 13:40
If you have been procrastinating on setting up electronic submissions for your adverse event reports to the FDA, you might want to reconsider that decision. Earlier this year, the FDA published its final rule on MedWatch/eMDR reporting.
Although…
