November 9-11, 2020 | Virtual Conference


Lina Cong

Regulatory Information Specialist, DDMSS, OBI, OSP, CDER

Lina Cong, Regulatory Information Specialist, FDA CDER, Office Business Informatics, eData team.  Ten years’ experience on study data standards, study data submission, and relevant guidance and policy in federal agency and ten years’ experience on clinical trial data analysis and clinical data management in pharmaceutical industry.

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