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INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT International Peer Reviewed & Refereed Journals, Open Access Journal ISSN Approved Journal No: 2456-4184 | Impact factor: 8.76 | ESTD Year: 2016 Scholarly open access journals, Peer-reviewed, and Refereed Journals, Impact factor 8.76 (Calculate by google scholar and Semantic Scholar | AI-Powered Research Tool) , Multidisciplinary, Monthly, Indexing in all major database & Metadata, Citation Generator, Digital Object Identifier(DOI) |
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| Paper Title: | VALIDATION AND DEVELOPMENT METHOD FOR THE ESTIMATION OF TEMOZOLOMIDE BY UV- SPECTROSCOPY |
| Authors Name: | Nellutla Sandeepthi , Nellutla Jhancy , Dr.B.Prabhakar Reddy , Dr.M.Srinivasa Murthy , B.sujan |
| Download E-Certificate: | Download |
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IJNRD_187466
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| Published Paper Id: | IJNRD2302167 |
| Published In: | Volume 8 Issue 2, February-2023 |
| DOI: | |
| Abstract: | Pharmaceutical analysis simply means analysis of pharmaceuticals. Webster’ dictionary defines a pharmaceutical is a medical drug. A more appropriate term for a pharmaceutical is active pharmaceutical ingredient (API) or active ingredient to distinguish it from a formulated product or drug product is prepared by formulating a drug substance with inert ingredient (excipient) to prepare a drug product that is suitable for administration to patients. Research and development (R&D) play a very comprehensive role in new drug development and follow up activities to ensure that a new drug product meets the established standards is stable and continue to approved by regulatory authorities ,assuring that all batches of drug product are made to the specific standards utilization of approved ingredients and production method becomes the responsibility of pharmaceutical analysts in the quality control (QC) or quality assurance department . The methods are generally developed in an analytical R&D department and transferred to QC or other departments as needed. At times they are transferred to other divisions. By now it should be quite apparent that pharmaceutical analysts play a major role in assuring the identity, safety, efficacy, and quality of drug product, safety and efficacy studies required that drug substance and drug product meet two critical requirements. 1. Established identity and purity. Established bio availability/dissolution |
| Keywords: | quality control (QC), identity and purity, Research and development (R&D), availability/dissolution, active pharmaceutical ingredients |
| Cite Article: | "VALIDATION AND DEVELOPMENT METHOD FOR THE ESTIMATION OF TEMOZOLOMIDE BY UV- SPECTROSCOPY", International Journal of Novel Research and Development (www.ijnrd.org), ISSN:2456-4184, Vol.8, Issue 2, page no.b683-b696, February-2023, Available :http://www.ijnrd.org/papers/IJNRD2302167.pdf |
| Downloads: | 000118752 |
| ISSN: |
2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar| ESTD YEAR: 2016 An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.76 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator |
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Published Paper ID:IJNRD2302167 Registration ID: 187466 Published In: Volume 8 Issue 2, February-2023 DOI (Digital Object Identifier): Page No: b683-b696 Country: Hyderabad, telangana, India Research Area: Pharmacy Publisher : IJ Publication Published Paper URL : https://www.ijnrd.org/viewpaperforall?paper=IJNRD2302167 Published Paper PDF: https://www.ijnrd.org/papers/IJNRD2302167 |
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