Theme:
Pharma Conference 2024
Welcome Message:
The 2nd Global Pharmaceutical & Pharma Industry Conference will be held in Dubai,UAE on April 18-19,2024. Confronting Global Issues and Exploring Scientific Inquiry on Pharmaceutics is the conference's key focus. It covers a variety of significant sessions. Inspiring Keynote Presentations, Plenary Talks, Symposiums, Special Sessions, and Career Development Programmes to make this top conference a success, we have thought of engaging workshops and keynote speakers.
The goal of the PHARMA CONFERENCE 2024 Professionals from the academic, pharmaceutical industry Research and Development wings, API: Active Pharmaceutical Ingredients industry, Drug discovery laboratories, Formulations and NDDS domains will also be attending the conference. This conference will also feature senior executives and renowned researchers from the fields of pharmaceutical chemistry, quality control, and assurance, clinical trials, pharmaceutical covigilance, pharmaceutical manufacturing, pharmacognosy, biopharmaceutics, drug discovery, design and development, and pharmacoeconomics.
Why to Attend?
The Pharma Conference 2024 will serve as a forum for discussion of new advancements in pharmaceutical science. The conference's characteristics include internationally renowned speakers, the most recent scientific discoveries, and consequently the most recent business developments in the pharmaceutical industry. The two-day event on pharmaceutical sciences may have more than 60 logical and focused talks and sub-sessions on cutting-edge global research projects in the subject. Find the most inventive and recent advancements in pharmaceutical technology and network with internationally renowned professionals and learn more about the direction and range of pharmaceutical investigations and talk about the development and importance of pharmaceutics amass and disseminate information.
Target Audience:
- Pharmacists
- Pharmaceutical Researchers
- Professors and Associate Professors
- Directors and CEO's of Organizations
- Pharmaceutical societies, Associations
- Physicians and clinical pharmacists
- Pharmacologists
- Nanotechnologists
- Pharma Researchers
- Pharma Scientist
- Pharmaceutical professionals (CEOs, MDs, Directors)
- Drug development and Discovery companies
- Pharmaceutical Associations and Societies
- Formulation and Pharma Manufacturing companies
- Medical Technology companies
- Chemist
- Microbiologist
- Biotechnologists
- Biochemist
- Post-Doctoral
- Health care Professionals
- Genomics ad Personalised medicines Experts
- Professors
- Industrial Experts
- Academicians
- Pharmaceutical Development companies
- Doctors
- Biomaterial scientists and Nanotechnologists
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Target Identification and Validation
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Preclinical Testing
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Clinical Trials
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Regulatory Approval
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Market Introduction
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Definition of Standards
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Process Monitoring
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Preventive Measures
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Documentation and Record Keeping
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Employee Training
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Customer Feedback and Satisfaction
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Continuous Improvement
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Compliance with Standards and Regulations
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Quality Control vs. Quality Assurance
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Automation in QA
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Biological Sources
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Types of Biopharmaceuticals
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Monoclonal antibodies
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Recombinant proteins
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Vaccines
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Gene therapies
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Nucleic acid-based therapies (RNA and DNA)
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Therapeutic Applications
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Biotechnological Production
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Regulation and Approval
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Challenges and Opportunities
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Cost and Accessibility
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Future Trends
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Technological Integration
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Process Optimization
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Customer-Centricity
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Data-Driven Decision-Making
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Agile and Innovative Culture
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Ecosystem Connectivity
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Cybersecurity and Risk Management
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Multi-Channel Engagement
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Adaptation to Change
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Strategic Planning
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Research and Development
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Clinical Trials and Regulatory Approval
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Knowledge Sharing and Data Exchange
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Public-Private Partnerships
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Supply Chain Collaboration
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Access to Medicines
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Vaccine Development and Distribution
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Healthcare Infrastructure Development
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Green Chemistry and Manufacturing
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Reducing Carbon Footprint
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Waste Reduction and Recycling
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Access to Medicines
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Research for Global Health
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Patient-Centric Sustainability
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Transparency and Reporting
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Stakeholder Engagement
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Patient Welfare
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Research Integrity
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Informed Consent
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Privacy and Confidentiality
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Fair Marketing Practices
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Access to Medicines
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Compliance with Regulations
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Anti-Bribery and Corruption
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Equitable Access to Clinical Trials
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Professional Integrity
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Increasing Healthcare Needs
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Rising Middle Class
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Access to Medicines
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Government Initiatives
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Clinical Trials and Research Opportunities
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Local Production and Manufacturing
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Partnerships and Collaborations
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Generic Drug Manufacturing
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Healthcare Infrastructure Investment
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Disease Prevention and Vaccination Programs
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Adverse Drug Reaction (ADR) Monitoring
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Data Collection and Analysis
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Signal Detection
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Risk Assessment and Management
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Regulatory Reporting
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Pharmacovigilance in Clinical Trials
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Pharmacovigilance in Herbal Medicines and Vaccines
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Technology and Automation
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Phases of Clinical Trials
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Informed Consent
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Randomized Controlled Trials (RCTs)
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Placebo-Controlled Trials
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Endpoints and Outcomes
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Principal Investigator (PI)
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Monitoring and Data Collection
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Regulatory Approval
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Patient Recruitment and Retention
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Post-Marketing Surveillance
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Drug Development and Formulation
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Raw Material Sourcing
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Quality Control and Assurance
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Granulation and Blending
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Tablet Compression or Capsule Filling
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Sterile Manufacturing
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Packaging and Labeling
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Quality Testing
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Regulatory Compliance
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Continuous Manufacturing
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Environmental Considerations
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Technology and Automation
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Supply Chain Management
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Genomic Information
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Biomarker Identification
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Targeted Therapies
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Pharmacogenomics
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Diagnostics and Imaging
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Tailored Treatment Plans
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Cancer Genomics
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Predictive Modeling
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Patient Engagement
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Preventive Medicine
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Challenges and Ethical Considerations
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Cost Considerations
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Disease Surveillance and Early Warning Systems
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Pandemic Preparedness
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Emergency Response Planning
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Public Health Infrastructure
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International Collaboration
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Capacity Building
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Vaccination Programs
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Risk Communication
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Research and Development
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Cross-Sectoral Collaboration
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Legal and Regulatory Frameworks
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Surge Capacity
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Resilience and Adaptability
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Cost-benefit analysis (CBA)
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Cost-Effectiveness Analysis (CEA)
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Cost-Utility Analysis (CUA)
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Budget Impact Analysis (BIA)
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Pharmacoeconomic Modeling
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Real-World Evidence (RWE)
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Quality of Life Assessment
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Patient-Reported Outcomes (PROs)
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Budget Constraints and Affordability
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Policy and Decision Support
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Market Access and Reimbursement
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Sensitivity Analysis
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Ethical Considerations
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Direct-to-Consumer Advertising (DTCA)
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Sales Representative Interactions
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Digital Marketing
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Medical Education and Continuing Medical Education (CME)
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Branding and Positioning
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Key Opinion Leader (KOL) Engagement
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Patient Support Programs
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Market Research
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Drug Discovery and Development
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Clinical Trials Optimization
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Personalized Medicine
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Drug Manufacturing and Quality Control
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Digital Health and Telemedicine
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Personalized Medicine
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Global Vaccination Initiatives
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Healthcare Data Analytics
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Patient-Centric Healthcare
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Value-Based Healthcare
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Rise of Biopharmaceuticals
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Global Health Security
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Regulatory Strategy Development
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Regulatory Submissions
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Clinical Trial Regulatory Compliance
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Quality Assurance and Good Manufacturing Practice (GMP)
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Post-Market Surveillance and Reporting
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Labeling and Packaging Compliance
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Regulatory Intelligence
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Interactions with Regulatory Agencies
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Regulatory Training and Education
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Regulatory Affairs in Medical Devices
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Orphan Drug Designation and Expedited Programs
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Drug Approval and Regulation
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Price Regulation and Access
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Intellectual Property Rights and Patents
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Generic Medicines Promotion
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Pharmacovigilance and Drug Safety
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Health Technology Assessment (HTA)
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Formulary Management
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R&D Incentives and Innovation
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Parallel Trade and Importation
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Pharmacy Practice and Distribution
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Pharmacy Education
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Pharmaceutical Science Education
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Pharmaceutical Technology and Manufacturing Education
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Clinical Research Education
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Regulatory Affairs Education
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Pharmacovigilance Training
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Health Economics and Outcomes Research (HEOR) Education
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Continuing Education
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Interdisciplinary Collaboration
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Global Health Perspectives
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Ethical and Regulatory Compliance Education
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Digital Platforms
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Digital Data
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Relative Bioavailability
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Genetic Phenotype
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Organ/tissue
Importance & Scope:
The finest venue for presenting and discussing contemporary aspects of drug development is the Pharma Conference 2022. Pharmacology is the study of how chemicals interact with biological things. To maximise the therapeutic benefits and lower the hazards for receivers of medications, it is crucial to talk about the pharmacological basis of therapies. As a result, it will be the ideal venue for academics, researchers, PhD candidates, graduates, and postgraduates working in the creation of new drugs
Global Pharmaceutical Chemicals Market: Key Research Aspects:
The pharmaceutical market is examined and predicted in this paper both globally and regionally. From 2017 through 2025, the market has been predicted based on volume (Tonnes) and revenue (US$ Mn), with 2016 serving as the base year. The worldwide pharmaceutical market's drivers and restraints are covered in the study. It also discusses how these factors will affect the forecasted demand for pharmaceuticals. The paper also identifies market prospects for pharmaceutical compounds both globally and locally.
Conference Highlights
- Pharmaceutical Innovation
- Technology in Pharma Sciences
- Novel Drug Delivery Systems, Biomarkers and Drug Targets
- Bioequivalence and Bioavailability
- Clinical Pharmacy and Pharmacy Practices
- Pharmacogenomics and Pharmacoepidemiology
- Pharmacology and Toxicology
- Pharmaceutical manufacturing and Pharmacoeconomics
- Digital Pharma and Marketing
- The future of Pharma R&D
- Pharmaceutical Analysis
- Nano medicine and Biomedical Application
- Drug Discovery, Design & Development: Challenges and Approaches
- Pharmaceutical Microbiology
- Pharmaceutical Nanotechnology
- Pharmaceutical Care and Health System
- Advanced Pharmaceutical Technology
- Drug Discovery
- Drug Discovery
- Pharmaceutical Innovation
- Pharmaceutical Innovation
To share your views and research, please click here to register for the Conference.
To Collaborate Scientific Professionals around the World
Conference Date | April 18-19, 2024 | ||
Sponsors & Exhibitors |
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Speaker Opportunity Closed | |||
Poster Opportunity Closed | Click Here to View |
Useful Links
Special Issues
All accepted abstracts will be published in respective Our International Journals.
Abstracts will be provided with Digital Object Identifier by