What Went Wrong? Pharma Tech Case Studies

What Went Wrong? Pharma Tech Case Studies (Hardcover, P G Shrotriya)

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What Went Wrong? Pharma Tech Case Studies  (Hardcover, P G Shrotriya)

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    Highlights
    • Binding: Hardcover
    • Publisher: Notion Press
    • Genre: MEDICAL / Reference
    • ISBN: 9781648997594
    • Edition: 1, 2020
    • Pages: 158
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  • Description
    The objective of What Went Wrong? Pharma Tech Case Studies is to provide multidisciplinary approaches/guidelines for problem-solving capability. These case studies are based on the actual situation faced by the author in India and overseas and successfully resolved with the back-up of science and technology convincing international regulators/complainants leading to the closing of complaints. The book provides guidelines covering regulatory requirements for documentation. How do you document (format) any complaint? How to investigate a case study, using knowledge of science and technology and method of investigation? How to reproduce the complaint in-house, where ever required? It answers these various questions. The conclusion is with corrective and preventive actions required, submission of the investigation report and assignable reason to the regulatory agency/complainant, getting a response from the complainant and once satisfied, requesting them to close the complaint. Can we integrate regulatory science with other subjects of pharmaceutical sciences to learn ‘What Went Wrong? In Pharma Tech Case Study’. Important regulatory references are provided at the end.
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    Book Details
    Publication Year
    • 2020
    Contributors
    Author Info
    • P G Shrotriya worked in different pharma industries for four decades in India and overseas, covering every facet of the industry. Being technically sound, he accepted challenging opportunities in international business. He headed the organisation that was the first to be successfully inspected and approved by the world’s highest inspecting authorities – the US FDA, UK MCA (present MHRA), followed by several international regulators, WHO, Australia TGA and Brazil ANVISA, to name a few. His technical expertise was acknowledged in WHO technical reports. He chaired the Parenteral Committee of Indian Pharmacopoeia 2010 and contributed to the Appendix in the National Formulary 2011. His expertise has been recognised internationally through invited lectures in China, USA, Japan, UAE, Italy, Russian countries, WHO, Ethiopia, to mention a few, besides regulatory bodies and academia in the country.
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