Case Studies | South Korea

US FDA
On-Time Literature Monitoring Services in the USA
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US FDA
One-Time Marketing Status Update to USFDA
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Multiple HAs
GPvP Audit in LATAM Region
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Health Canada
Successful DMF Submission to the Health Canada
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US FDA
Comprehensive Gap Analysis and Successful Submission to the USFDA
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US FDA
Submission of CBE 30 within 3 days
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Health Canada
Successful DMF submissions Within One Week With 70% Cost Benefits
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MFDS
Regulatory Assessment of Ingredients as per the MFDS Guidelines
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US FDA
Product Correspondence for USA Agent Change
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