Compare US and EU IND Submission Process
Palash Chandra Das
SME In - Sterility Assurance Engineering | investigation | Risk Management | Regulatory inspection & Compliance (USFDA, EU) | Manufacturing science and technology | R&D | Quality | Validation | CAPA |
Please note that this table provides a general overview, and the specifics may vary based on the type of drug, therapeutic area, and other factors. Additionally, regulatory processes are subject to updates and changes, so it's crucial to refer to the latest guidelines from the EMA and FDA for the most accurate and current information.