Regulatory Affairs Intern at GSK with hands-on experience in Veeva Vault (25.1). Proven ability to manage regulatory information, improve data accuracy, and support process efficiency. Skilled in regulatory documentation, compliance monitoring, and policy analysis. Strong communicator with a collaborative and adaptable approach to problem-solving and ensuring smooth regulatory processes and adherence to guidelines. and also eager to contribute to Regulatory Submission Excellence, CMC, and Submission & Publication activities.
Pharmacological Evaluation of Chrysin Loaded Phytosomes against Breast Cancer Analytical Dissolution Method Development and Validation for H2-receptor antagonist Oral Suspension by HPLC Dissolution Method Development for Nisoldipine Tablets by UV
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