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Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|January 15, 2011
Recombinant drug development, regulation, and commercialization: an Indian industry perspectiveNiharika Sahoo, Padmavati ManchikantiMedical Law Review|August 24, 2023
Post-trial access to investigational drugs in India: addressing challenges in the regulatory frameworkNidhi Mehrotra, Padmavati ManchikantiJournal of Alternative and Complementary Medicine (New York, N.Y.)|July 9, 2013
Herbal drug regulation and commercialization: an Indian industry perspectiveNiharika Sahoo, Padmavati ManchikantiPharmaceutical Research|December 10, 2025
From Clinical Trials to Commercialization: Perspectives in Human VaccineNidhi Mehrotra, Padmavati ManchikantiPharmaceutical Medicine|January 24, 2024
Emergency Approval Mechanisms for Human Vaccines in IndiaNidhi Mehrotra, Padmavati ManchikantiBiodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|August 25, 2009
Manufacturing of biodrugs: need for harmonization in regulatory standardsNiharika Sahoo, Koel Choudhury, Padmavati ManchikantiFitoterapia|February 17, 2010
Herbal drugs: standards and regulationNiharika Sahoo, Padmavati Manchikanti, Satyahari DeyJournal of Ethnopharmacology|June 7, 2011
Herbal drug patenting in India: IP potentialNiharika Sahoo, Padmavati Manchikanti, Satya Hari DeyRecent Patents on Biotechnology|November 25, 2016
Patents in Nanobiotechnology: A Cross Jurisdictional ApproachPadmavati Manchikanti, Shailaja Uppala, Ramesh Kumar BontaJournal of Food Science and Technology|April 19, 2018
Identification and characterization of bioactive phenolic constituents, anti-proliferative, and anti-angiogenic activity of stem extracts of <i>Basella alba and rubra</i>B Ramesh Kumar, Apoorva Anupam, Padmavati Manchikanti, et al.Pageof 2