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Regulatory affairs course
What a regulatory file is, and what the regulatory affairs page at PharmaWiz says about the course.
What regulatory affairs is
Before a company studies a medicine, and again before it sells one, it files documents with a regulator. Regulatory affairs is the work of preparing and tracking those documents: what the product is, what the trial showed, and which form the authority asked for.
What this course page lists
The regulatory affairs page calls it training inside ASCEND, with mentor Ameeroddin Mohammad. The curriculum headings on the page start with an introduction to regulatory affairs, clinical trials and phases, and drug discovery and development. Eligibility is the same line as the other courses: B.Pharm, M.Pharm, Pharm D and life sciences graduates. The site FAQ says the October 2026 ads describe regulatory affairs as about 30 hours.
Where the classroom is
PharmaWiz teaches at MIG 1-187, 2nd Floor, R.R. Chandana Residency, KPHB Phase-I, Road No. 1, Hyderabad 500072. ASCEND can also be taken live on Microsoft Teams.