Radhika Singh

• Supported the Quality Control department to ensure compliance with internal and regulatory quality standards
• Developed working knowledge of Good Manufacturing Practices (GMP) and Quality Assurance (QA) processes
• Assisted in preparing documentation and maintaining QA records to facilitate regulatory audits

Main Project: Assessment of Commercially Available In-Home Drug Disposal Product

• Lead research evaluating drug disposal kit effectiveness through analytical testing.
• Assess product performance, safety, and regulatory implications.
• Contributing author on upcoming publication based on study findings.

Additional Research Contributions:

• Conduct dissolution/disintegration testing on oral solid dosage forms to evaluate performance.
• Perform stability studies under ICH guidelines to assess shelf life and formulation integrity.
• Quantify APIs and degradation products using UPLC under GLP-compliant methods.
• Document results and maintain laboratory notebooks in line with SOP and GLP standards.
• Collaborate with multidisciplinary team on formulation and method development discussions.