Regulatory Affairs Specialists in toxicology have a broad range of responsibilities, including:
1. Regulatory Compliance: Ensuring that all products meet the necessary regulatory requirements for safety and efficacy. 2. Documentation and Submissions: Preparing and submitting regulatory documents, such as Investigational New Drug (IND) applications and New Drug Applications (NDA). 3. Risk Assessment: Conducting risk assessments to evaluate the potential health impacts of chemical substances. 4. Labeling and Packaging: Ensuring that all product labeling and packaging comply with regulatory standards. 5. Liaison: Acting as a liaison between the company and regulatory agencies. 6. Staying Updated: Keeping abreast of changes in laws and regulations that affect product safety.
