What are the major responsibilities of DST?
The question appears to conflate two distinct entities: "DST" and "Drugs Regulatory Affairs." It's not clear what "DST" stands for in this context, and there may be some confusion.
If we assume that "DST" refers to a regulatory authority or department related to drugs, I can provide a general answer related to the responsibilities of a Drugs Regulatory Affairs department within a regulatory agency or pharmaceutical company.
Drugs Regulatory Affairs Responsibilities:
1. Regulatory Submissions: Regulatory affairs professionals are responsible for preparing and submitting regulatory documents to obtain approvals, licenses, and permits for the development, production, and marketing of drugs. This includes applications for clinical trials, new drug approvals, and post-marketing approvals.
2. Compliance: Ensuring that all activities related to drug development, manufacturing, and distribution
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