Dr. Anushka Dubey is a committed pharmaceutical professional and researcher with hands-on experience in regulatory affairs, quality assurance, and training coordination. Currently serving as a Quality Assurance Officer at Umedica Laboratories, she is engaged in regulatory documentation, pharmacovigilance protocols, and quality management processes. She has also served as a trainer and training coordinator at PTE Universe, showcasing her versatility across technical and educational domains.
Her current responsibilities encompass a wide range of regulatory and documentation activities including:
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Submission of ANDA and other regulatory documents
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Preparation and review of Pharmacovigilance (PV) and Hold Time (HT) protocols
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Management of SOPs, change control, deviation, CAPA, and document lifecycle in EQMS/EDMS systems
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Control sample handling, logbook issuance, and specification/STP documentation for QC
Significant Achievements
Dr. Dubey has contributed extensively to scientific literature with multiple research publications in reputed national and international journals. Her work demonstrates a strong focus on pharmacovigilance, adverse drug reactions, antibiotic resistance, and medico-legal implications.
Her notable publications include:
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"URGE TO STEAL VERSUS URGE TO FIRE – Medico Legal Pertinence" (IJRAR, 2023)
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"Cystic Fibrosis Medication Causing Antibiotic Resistance" (IJMSCRR, 2024)
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"An Ambispective Study on Adverse Drug Reactions in a Tertiary Care Teaching Hospital" (Asian J. Res. Pharm. Sci., 2025)
She also participated in a retrospective pharmacovigilance research project focused on monitoring adverse drug reactions at a tertiary care teaching hospital, underlining her dedication to improving drug safety and public health outcomes.
Notable Contributions
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Demonstrated competence in regulatory submissions and quality assurance systems
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Active contribution to pharmacovigilance and medication safety research
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Engaged in training and coordination, enhancing the professional development of others
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Played an essential role in document control, compliance, and quality documentation systems in the pharmaceutical manufacturing environment
Eligibility for Women Researcher Award
With her growing research portfolio, multidisciplinary skills, and active contributions in pharmaceutical quality systems and clinical safety research, Dr. Anushka Dubey is eligible to receive the "Women Researcher Award" in Scientific Laurels. Her commitment to scientific integrity, regulatory compliance, and patient safety positions her as a rising talent in the pharmaceutical and medical research domains.