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Clinical Research5 Best Practices to Follow While Budgeting for a Clinical Trial -
Food Safety ComplianceHACCP - 5 Record Keeping Best Practices to Ensure Compliance -
HR ComplianceFair Labor Standards Act-What Employers Need to Know -
Banking and Financial ServicesBank Secrecy Act - 6 Key Best Practices to Ensure ... -
All FDA Regulated IndustryFDA Current Good Manufacturing Practices ... -
Risk ManagementCreating Effective ERM Program ... -
Medical DevicesThe 510(k) Application - 5 Best Practices Medical Device ... -
BiotechnologyRisk Factors Associated with Immunogenicity Testing
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ComplianceOnline GRC Best Practices
Get trained on regulations affecting your industry through online webinars, learn the best practices, and download quality standards, checklists and news articles. Listen to experts on best practices to streamline quality and compliance processes and meet the regulatory demands.Most Read
FDA Current Good Manufacturing Practices (cGMPs) for Finished Pharmaceuticals
Current Good Manufacturing Practices are regulations published by FDA to provide criteria for complying with the Federal Food, Drug, and Cosmetic Act (FD&C Act)...
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National Aeronautics and Space Administration Authorization Act of 2010
The National Aeronautics and Space Administration Authorization Act of 2010 is a bill that supports the overall growth of science, aeronautics, and space technology. It defines long-term goals ...
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FDIC Guidance on Safeguarding Customers against E-Mail and Internet-Related Fraudulent Schemes - Best Practices to Follow
According to the Internet Crime Complaint Center (IC3) (partnership between the Federal Bureau of Investigation and the National White Collar Crime...
ComplianceOnline
Creating Effective ERM Program
The variety and complexity of risks facing today's organizations is increasing due to emerging technologies, globalization, and increased compliance obligations. The financial market breakdown of 2007/08 has emphasized the importance of...
ComplianceOnline
Medical Device Reporting for Manufacturers - Best Practices to Follow
The FDA requires medical device manufacturers to submit reports in case of device malfunctioning. But when and how are these reports to be submitted? Which medical device...
ComplianceOnline
Adverse Event Reporting to IRBs - Best Practices to Follow
The Food and Drug Administration (FDA) has issued guidelines for adverse event reporting because adverse event reports were found to be inhibiting, rather than enhancing, the ability of IRBs to protect the human subjects. This article describes the best...
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