Upcoming Workshop

• Writing Technical Regulatory Documents
• eCTD Submission to the US FDA 
• FDA GMP for Phase I and First-in-Man Clinical Trials
• SOPs for FDA-Regulated Industry                                 Click for More...

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For additional information on the workshop agenda and logistics, please call +1 410-501-5777 or +1 877-566-4981 or email: [email protected]