NBFCs: Regulatory framework in India

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Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας:	GUPTA,RHEA MANGAL
Μορφή:	Thesis Βιβλίο
Γλώσσα:	Αγγλικά
Έκδοση:	Mumbai NMIMS Mumbai 2022
Θέματα:	Regulatory framework
Ετικέτες:	Προσθήκη ετικέτας Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!

Παρόμοια τεκμήρια

A Comparative Study of Regulatory Framework of Mergers & Acquisitions in India & USA
από: Shah, Ishani
Έκδοση: (2022)

Part I - Regulatory Framework for Development of Paediatric Formulations Part II - Exploring Regulatory Submissions in Emerging Market
από: Dand Chandni

"Part I - Regulatory Framework for Coronary Stents in Regulated and Semi- Regulated Countries. Part II - Understanding Regulatory Submissions: Ensuring Global Regulatory Compliance"
από: Tyagi Somya

"Part I - Analysis of Regulatory framework for Nanopharmaceuticals in the US, EU and India. Part II - Regulatory Affairs and Dossier Management at Cipla Ltd"
από: Patel Aiman

Part I Real World Evidence for Regulatory Decision Making: Indian Framework Part II Navigating the USFDA Regulatory Landscape: Insights from Theory to Application
από: Gupta Adarsh

"Part I Regulatory Policy Framework for Entrepreneurship with Pharmaceutical Avenues Part II Hands-On Experience at Regulatory Affairs Department of Cipla"
από: Vasmatkar Mahesh

"Part I - Regulatory Considerations of Nitrosamines: Exploring Mutagenic and Impurities and Genotoxicity in Pharmaceuticals Part II - Navigating Regulatory Frameworks : A practical Approach To Global Compliance"
από: Gharat Sejal

"Part I - Regulatory Framework and Market Dynamics of Nutraceuticals in Major International Markets Part II - Developing Dossier and Regulatory Submission Strategies for Pharmaceutical Market Authorization in the European Union."
από: Bose Anushree

"Part I - Regulatory Framework and Innovations using 505(b)(2) Pathway in Drug Development and Approval Part II - Internship at Bliss GVS Pharma in Regulatory Affairs Department- US Market"
από: Patel Astha

"Part I - Eurasian Economic Union: Analyzing Drug Registration Pathways, Dossier Requirements and Comparison with European Union's Regulatory Frameworks Part II - Implementation of Regulatory Practices for Pharmaceutical Submission in the European Union"
από: CP Keerthana

"Part I - Regulatory Considerations for Biologics Approval Processes in USA, India and EU Part II - Exploring Regulatory Affairs and Global Submissions "
από: Pawar Srushti

FDA REGULATORY AFFAIRS
από: MANTUS DAVID
Έκδοση: (2021)

Pharmaceutical Regulatory Process,
από: Berry I.R
Έκδοση: (2025)

Drug Regulatory Affairs
από: Itkar, Sachin
Έκδοση: (2022)

Drug Regulatory Affairs
από: Singh
Έκδοση: (2023)

Drug Regulatory Affairs
από: Gajendra
Έκδοση: (2023)

Part I - Regulatory Frameworks for Generic Drug Applications and to Identify the Filing Discrepancies Part II - Internship Experience: Documents Required, dossier Preparation and Deficiency Analysis
από: Pawar Jyoti

Part I Regulatory Considerations and Comparison of Drug Product Recall For Nitrosamine Impurity In India, USA And Europe Part II Navigating Regulatory Framework: A Strategic Approach in Industry"
από: Mutalik Rucha

Regulation and Regulatory Process in India
από: Kumar, Manoj
Έκδοση: (2019)

Drug Regulatory Affairs (PB)
από: Bigoniya
Έκδοση: (2019)

"Part I Nisin-Silver Nanoconjugate in Polymeric Microneedles for Antimicrobial Action and Regulatory Aspects of Microneedles in India, USA and Europe Part II Navigating USFDA and CDSCO Regulatory Requirements and Hadling the Documentation Approaches"
από: Domb Dnyaneshwari

"Part I Comparison of Regulatory Considerations for Repurposed Drugs in US, EU, & India Part II Optimizing Regulatory Processes Enhancing Product Life Cycle Management from Initial Filimg to Post-Approval"
από: Bajaj Aanchal

"Part I - Regulatory Perspective and Strategies to Strength and Speed Ip Commercialization Process Part II - Dossier Preparation and Regulatory Compilance in ROW: A Pratical Approach in Ajanta Pharma"
από: Dwivedi Priyam

"A Textbook of Pharmaceutical Regulatory Science"
από: Mrs. Mitesh P. Sonawane
Έκδοση: (2022)

"Part I - Regulatory Framework for the Novel Polymers and Features of Approved Polymers in Orally Disintegrating Tablets as per U.S. FDA Part II - Preparation of Module 3 for the Submission of ANDA in the U.S. Market at Bliss GVS Pharma Ltd"
από: Shetty Kavyashree

"Part I - Regulatory Compliance Leveraging Artificial Intelligence - A comprehensive Study of Opportunities and Challenges Part II - From Analytical Profiling to Regulatory Affairs - Stability, Assessment, Forced Degradation and RA Submissions for Emerging Markets "
από: Mulla Sahil

"Part I - Regulatory Aspects for Zygomatic Implants as Medical Devices in India Part II - Internship at Meril Life Sciences Pvt. Ltd & IPCA Laboratories Ltd"
από: Mistry Yukta

"Part I Regulatory Pathway And Formulation Strategy For 505(B)(2) Filing Of Oral Dispersible Strips In Anti-Epileptic Therapy Part II Navigating the Regulatory Compliance at Glaxosmith Kline Pharmaceuticals Limited for General Medicine Products Concerning Licenses and Best Practices"
από: Nair Keerthi

Legal and Regulatory Aspects of Banking
από: Zacharias, K D; Ravindranath, C P; Kulkarni, P R; Gopalakris
Έκδοση: (2008)

Legal and Regulatory Aspects of Banking
από: Zacharias, K D; Ravindranath, C P; Kulkarni, P R; Gopalakris
Έκδοση: (2008)

Legal and Regulatory Aspects of Banking
από: IIBF
Έκδοση: (2012)

"Part I Regulatory Analysis and Comparison of Medical Device Recall In India, US and Europe: Understanding Causes and Consequences. Part II Dossier Preparation and Submission for US Market in Sun Pharmaceutical Industries"
από: Bodke Samruddhi

"Part I Exploring The Regulatory Dynamics Of Artificial Intelligence (AI) and Machine Learning(ML) Based Smart Devices Part II Navigating Though the Reglatory Compliances at Glaxosmithkline Pharmaceuticals Limited for Clinical Trials in India"
από: Mourya Aman

"Part I Regulatory Considerations and In-Silico Exploration of Cetilistat in The Treatment Of Non-Alcoholic Fatty Liver Disease Part II Preparation and Documentation of Device Master File"
από: Vasekar Amey

Part I Regulatory Scenario Of 3D Bioprinting In Developed And Developing Countries. Part II Exploring the Frontiers of Clinical Research: Insights at a Contract Research Organization
από: Desai Rutuja

Part I - Harmonisation of Orphan Drug Regulations: Comparing Indian Regulations with US and EU Regulations Part II - Internship Experience Document Review, Dossier Compliation Process for Regulatory Submission in Iraq
από: Gubare Uddesh

Part I - Comprehensive Evaluation of Food Defects as per FDA: A Statistical Analysis Part II - Global Regulatory Affairs: A Practical Approach to Dossier Preparration, Gap Analysis, Query Resolution and Documentation
από: Pawnikar Vaishnavi

"Part I Financial Implications of Non-Compliance with U.S. F.D.A. Regulations on CGMP for Finished Pharmaceutical Products: A Case Study Analysis Part II Exploring the U.S.F.D.A. Regulatory Pathways"
από: Shetty Samiksha

Guide to drug regulatory affairs
από: Friese,Brigitte
Έκδοση: (2007)

Regulation And Regulatory Process In India
από: Kumar, Manoj
Έκδοση: (2019)