Resultados da pesquisa - "Affaires"

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  1. 1
    "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"

    "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 Glaxos... Por Mourya Aman

    Assuntos: “...Regulatory Affairs...”
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  2. 2
    "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"

    "Part I - Eurasian Economic Union: Analyzing Drug Registration Pathways, Dossier Requirements and Comparison with European Union's Regulatory Frameworks Part II - Implementation o... Por CP Keerthana

    Assuntos: “...Regulatory Affairs...”
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  3. 3
    "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"

    "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 S... Por Shetty Kavyashree

    Assuntos: “...Regulatory Affairs...”
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  4. 4
    "Part I - Regulatory Framework for Coronary Stents in Regulated and Semi- Regulated Countries. Part II - Understanding Regulatory Submissions: Ensuring Global Regulatory Compliance"

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

    Assuntos: “...Regulatory Affairs...”
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  5. 5
    "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 "

    "Part I - Regulatory Compliance Leveraging Artificial Intelligence - A comprehensive Study of Opportunities and Challenges Part II - From Analytical Profiling to Regulatory Affai... Por Mulla Sahil

    Assuntos: “...Regulatory Affairs...”
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  6. 6
    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

    Part I - Regulatory Frameworks for Generic Drug Applications and to Identify the Filing Discrepancies Part II - Internship Experience:... Por Pawar Jyoti

    Assuntos: “...Regulatory Affairs...”
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  7. 7
    "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."

    "Part I - Regulatory Framework and Market Dynamics of Nutraceuticals in Major International Markets Part II - Developing Dossier and Regulatory Submission Strategies for Pharmaceut... Por Bose Anushree

    Assuntos: “...Regulatory Affairs...”
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  8. 8
    Part I - Regulatory Framework for Development of Paediatric Formulations Part II - Exploring Regulatory Submissions in Emerging Market

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

    Assuntos: “...Regulatory Affairs...”
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  9. 9
    "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"

    "Part I - Regulatory Considerations of Nitrosamines: Exploring Mutagenic and Impurities and Genotoxicity in Pharmaceuticals Part II - Navigating Regulatory Frameworks : A practica... Por Gharat Sejal

    Assuntos: “...Regulatory Affairs...”
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  10. 10
    "Part I - Analysis of Regulatory framework for Nanopharmaceuticals in the US, EU and India. Part II - Regulatory Affairs and Dossier Management at Cipla Ltd"

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

    Assuntos: “...Regulatory Affairs...”
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  11. 11
    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

    Part I - Harmonisation of Orphan Drug Regulations: Comparing Indian Regulations with US and EU Regulations Part II - Internship Experience Document Review, Dossier Compliation Pr... Por Gubare Uddesh

    Assuntos: “...Regulatory Affairs...”
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  12. 12
    "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"

    "Part I - Regulatory Perspective and Strategies to Strength and Speed Ip Commercialization Process Part II - Dossier Preparation and Regulatory Compilance in ROW: A Pratical Appro... Por Dwivedi Priyam

    Assuntos: “...Regulatory Affairs...”
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  13. 13
    "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"

    "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-... Por Patel Astha

    Assuntos: “...Regulatory Affairs...”
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  14. 14
    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

    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... Por Pawnikar Vaishnavi

    Assuntos: “...Regulatory Affairs...”
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  15. 15
    "Part I - Regulatory Aspects for Zygomatic Implants as Medical Devices in India Part II - Internship at Meril Life Sciences Pvt. Ltd & IPCA Laboratories Ltd"

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

    Assuntos: “...Regulatory Affairs...”
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  16. 16
    "Part I - Regulatory Considerations for Biologics Approval Processes in USA, India and EU Part II - Exploring Regulatory Affairs and Global Submissions "

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

    Assuntos: “...Regulatory Affairs...”
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  17. 17
    Part I A Comparative Analysis of Medical Device Regulations in Emerging ASEAN Markets and India Part II Ensuring Compliance and Efficacy: A Statergic Approach to Executive Quality Assurance in Bioavailibilty and Bioequivalance Study

    Part I A Comparative Analysis of Medical Device Regulations in Emerging ASEAN Markets and India Part II Ensuring Compliance and Efficacy: A Statergic Approach to Executive Quality... Por Jadhav Archana

    Assuntos: “...Regulatory Affairs 926...”
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  18. 18
    Part I Analysing Regulatory Pathways and Approval Processes for Spinal Orthopedic Implants: A Comparative Study of USA, EU And India Part II Preparing And Reviewing Dossier for Venezuela Country

    Part I Analysing Regulatory Pathways and Approval Processes for Spinal Orthopedic Implants: A Comparative Study of USA, EU And India Part II Preparing And Reviewing Dossier fo... Por Pawar Himanshu

    Assuntos: “...Regulatory Affairs 928...”
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  19. 19
    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"

    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 Approa... Por Mutalik Rucha

    Assuntos: “...Regulatory Affairs 930...”
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  20. 20
    "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"

    "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 Glaxos... Por Nair Keerthi

    Assuntos: “...Regulatory Affairs...”
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