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ComplianceQuest

10006 cross creek Blvd, suite 71, AbuDhabi 4084588343 https://www.compliancequest.com
The FDA Adverse Event Reporting System (FAERS) is a publicly available database containing information on adverse events and medication error reports submitted to FDA.
The FDA Adverse Event Reporting System (FAERS) is a publicly available database containing information on adverse events and medication error reports submitted to FDA.

It significantly improve an organization’s culture, collaboration, competency, efficiency, performance and innovation through the digital transformation of quality, health, safety and compliance delivered via 100% Salesforce powered cloud based QHSE solutions.

Our connected suite of solutions helps businesses of all sizes increase quality, safety and efficiency as they bring their products from concept to customer success. Our intelligent data-driven platform comes with best-in-class integrated processes to mitigate risks, protecting your employees, suppliers and brand reputation, and to increase innovation, compliance, profit and customer loyalty. ComplianceQuest is pre-validated and easy to implement, use, and maintain, allowing for streamlined communication and collaboration across the product value chain.

We Create an Environment of Trust by Goal Oriented continually focusing on increasing productivity and reducing costs .

Email [email protected]
fda adverse event reporting system

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