Vol. 11 No. 02 (2023): JPBR

Articles

• A Study on medical devices as per EU and CHINA

  Gudapati Sirisha, Yarra Sai Phanindra, Adapa Haritha Naga Vara Lakshmi, Doonaboyina Raghava (Author)

  43-46

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• Current Research and Regulatory Steps for Further Development of Clinical Trials in India

  Kotipalli Jyothirmaye, Yarra Sai Phanindra, Beram Saranya, Doonaboyina Raghava, Kavala Nageswara Rao (Author)

  47-51

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• Formulation development and in-vitro evaluation of controlled release dalfampridine hydrogel beads

  Maddala Anitha, Bhogireddi Sriswetha, D. Raghava, K. Nageswara Rao (Author)

  52-55

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• Formulation, Development and In-Vitro studies of Sotalol - Gastro Retentive Floating tablets

  K. Jacob Isaac, BH. Sri Swetha, D. Raghava, K. Nageswara Rao (Author)

  56-60

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• Regulatory Requirement for the Quality Improvement Plan for a Stabilized Product Development

  Nandini Ramani, Y. Sai Phanendra, G. Sirisha, Doonaboyina Ragava, Kavala Nageswara Rao (Author)

  61-64

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• A Study on Medical Device Regulations Related to their Warning Letters and Product Recals in Association of Southeast Nations

  Bhavitha Gogula, Y. Sai Phanendra, Adapa Haritha Naga Vara Lakshmi, Doonaboyina Ragava, Kavala Nageswara Rao (Author)

  65-73

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• Assessment of Regulatory Requirements and Filling Procedure of Drug Master File for Brazil, Europe, and India, USA and Australia

  M.N. Shankarananda, K. Sunil Kumar (Author)

  74-82

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