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Call For Abstract | pharmaceutical Conferences | Dubai | 2024
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text-right text-shadow h3"> <strong class="text-success ">Dec 05-06, 2024 </strong><br> <span class="text-primary">Dubai , UAE</span> </p> </div> </div> </div> </div> </header><div class="main-content"> <div class ="container"> <h2 class="text-uppercase text-center h3">Track Categories</h2> <div class="row"> <div class="col-md-9"> <p>The track category is the heading under which your abstract will be reviewed and later published in the conference printed matters if accepted. During the submission process, you will be asked to select one track category for your abstract. </p> <div class="panel-group tracks" id="accordion"> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse1"> <span> Track 1 : </span>Target Identification & Validation </a> </h4> </div> <div id="collapse1" class="panel-collapse collapse in"> <div class="panel-body"> <p><p> 1.<a href="https://dermatology.pulsusconference.com/abstract-submission"><strong>Target Identification & Validation</strong></a>:</p> <p> This session delves into cutting-edge techniques and strategies to identify and validate promising <a href="https://pharmaceutics.cmesociety.com/abstract-submission">drug targets</a>, including genomics, proteomics, and <a href="https://pharmaceutics.cmesociety.com/about-us">bioinformatics</a> approaches. It aims to accelerate <a href="https://pharmaceutics.cmesociety.com/about-us">drug</a> discovery by pinpointing the most relevant <a href="https://pharmaceutics.cmesociety.com/abstract-submission">therapeutic targets</a> for various diseases.</p> <p> 1-1 <a href="https://pharmaceutics.cmesociety.com/registration">Genomics</a> in target discovery</p> <p> 1-2 Proteomics and <a href="https://pharmaceutics.cmesociety.com/organizing-committee">drug </a>targets</p> <p> 1-3 <a href="https://pharmaceutics.cmesociety.com/about-us">Bioinformatics</a> approaches</p> <p> 1-4 Functional Genomics for Target Validation</p> <p> 1-5 Artificial Intelligence and Machine Learning in <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Target Discovery</a> and Validation</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse2"> <span> Track 2 : </span> .Hit-to-Lead Optimization: </a> </h4> </div> <div id="collapse2" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 2. <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Hit-to-Lead Optimization</a>:</p> <p style="text-align: justify;"> Delve into the unveils the transformative journey of turning promising <a href="https://pharmaceutics.cmesociety.com/about-us">drug</a> candidates into potential therapies. Explore advanced strategies and techniques in medicinal chemistry and <a href="https://pharmaceutics.cmesociety.com/about-us"> drug, </a> <a href="https://pharmaceutics.cmesociety.com/about-us">design</a> to refine initial compounds for enhanced potency, safety, and selectivity, propelling them towards clinical development</p> <p style="text-align: justify;"> 2-1Structure-based<a href="https://pharmaceutics.cmesociety.com/abstract-submission"> drug </a><a href="https://pharmaceutics.cmesociety.com/about-us">desig</a></p> <p style="text-align: justify;"> 2-2High-throughput screening</p> <p style="text-align: justify;"> 2-3<a href="https://pharmaceutics.cmesociety.com/organizing-committee">Medicinal chemistry</a> strategies</p> <p style="text-align: justify;"> 2-4 Fragment-Based <a href="https://pharmaceutics.cmesociety.com/abstract-submission">drug </a>Discovery</p> <p style="text-align: justify;"> 2-5In silico <a href="https://pharmaceutics.cmesociety.com/about-us">drug, </a><a href="https://pharmaceutics.cmesociety.com/about-us">design</a> and Virtual Screening</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse3"> <span> Track 3 : </span> Preclinical Development: </a> </h4> </div> <div id="collapse3" class="panel-collapse collapse "> <div class="panel-body"> <p><p> <strong>3 . </strong><a href="https://pharmaceutics.cmesociety.com/call-for-abstracts"><strong>Preclinical Development</strong></a><strong>:</strong></p> <p> Embark on the crucial journey from laboratory to clinic. This session explores the meticulous process of evaluating <a href="https://pharmaceutics.cmesociety.com/about-us"> drug, </a> candidates in animal models, ensuring safety and efficacy before human trials. Delve into <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmacology</a>, toxicology, and pharmacokinetic studies that lay the foundation for successful <a href="https://pharmaceutics.cmesociety.com/organizing-committee">drug </a>development<strong>.</strong></p> <p> 3-1 Animal models for drug testing</p> <p> 3-2 In vitro <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmacology</a> studies</p> <p> 3-3 Preclinical safety assessment</p> <p> 3-4 Pharmacokinetics and <a href="https://pharmaceutics.cmesociety.com/about-us">Metabolism</a> Studies (PK/DM)</p> <p> 3-5 Formulation Development and Optimization</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse4"> <span> Track 4 : </span>Clinical Trial design & Management: </a> </h4> </div> <div id="collapse4" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 4 .<a href="https://pharmaceutics.cmesociety.com/about-us"><strong>Clinical Trial </strong><u>design</u> <strong>& Management:</strong></a></p> <p style="text-align: justify;"> Navigate the intricate landscape of <a href="https://pharmaceutics.cmesociety.com/abstract-submission"><u>clinical trials</u>.</a> This session unveils the art and science of design ing robust studies, ensuring regulatory compliance, recruiting diverse patient populations, and analyzing data to determine the safety and efficacy of new <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a> interventions.</p> <p style="text-align: justify;"> 4-1 <a href="https://pharmaceutics.cmesociety.com/">Phase I-IV trial</a> <a href="https://pharmaceutics.cmesociety.com/about-us">design</a></p> <p style="text-align: justify;"> 4-2 Endpoint selection and validation</p> <p style="text-align: justify;"> 4-3 Patient recruitment and retention</p> <p style="text-align: justify;"> 4-4 Clinical Trial Operations and Logistics</p> <p style="text-align: justify;"> 4-5Patient-Reported Outcomes (PROs) and <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Quality of Life</a> Assessments</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse5"> <span> Track 5 : </span>Regulatory Affairs & Market Approval: </a> </h4> </div> <div id="collapse5" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 5 .<a href="https://pharmaceutics.cmesociety.com/registration"><strong>Regulatory Affairs & Market Approval:</strong></a></p> <p style="text-align: justify;"> Unlock the pathway to global markets. This session demystifies the intricate regulatory landscape, guiding you through successful submissions and post-marketing strategies to ensure your <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a> innovation reaches patients worldwide.</p> <p style="text-align: justify;"> 5-1 Regulatory submission strategies</p> <p style="text-align: justify;"> 5-2 Post-market safety monitoring</p> <p style="text-align: justify;"> 5-3 Global regulatory landscape</p> <p style="text-align: justify;"> 5-4 Intellectual Property (IP) and Regulatory Strategies</p> <p style="text-align: justify;"> <strong>5-5 Evolving Regulatory Landscape for Cell and </strong><a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Gene Therapies</a></p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse6"> <span> Track 6 : </span>Synthesis & Process Chemistry: </a> </h4> </div> <div id="collapse6" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 6.<a href="https://dermatology.pulsusconference.com/abstract-submission"><strong> Synthesis & Process Chemistry</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Unlock the pathway to global markets. This session demystifies the intricate regulatory landscape, guiding you through successful submissions and post-marketing strategies to ensure your<a href="https://pharmaceutics.cmesociety.com/abstract-submission"> <u>pharmaceutical</u></a> innovation reaches patients worldwide.</p> <p style="text-align: justify;"> 6-1 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Novel synthesis</a> routes</p> <p style="text-align: justify;"> 6-2 Green chemistry in <a href="https://pharmaceutics.cmesociety.com/about-us">Pharma</a></p> <p style="text-align: justify;"> 6-3 Scaling up Drug production</p> <p style="text-align: justify;"> 6-4 Continuous Manufacturing and Process Intensification</p> <p style="text-align: justify;"> 6-5 Quality by design (QbD) and Process Analytical Technology (PAT</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse7"> <span> Track 7 : </span> Formulation Development: </a> </h4> </div> <div id="collapse7" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 7. <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts"><strong>Formulation Development</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Elevate the delivery of therapeutic innovation. This session explores the intricate science of crafting optimal<a href="https://pharmaceutics.cmesociety.com/registration"> Drug</a> formulations, ensuring effective absorption, stability, and bioavailability across diverse delivery routes, ultimately maximizing patient benefit.</p> <p style="text-align: justify;"> 7-1 Oral <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">drug delivery</a> optimization</p> <p style="text-align: justify;"> 7-2 Injectable formulations</p> <p style="text-align: justify;"> 7-3 Stability testing and formulation</p> <p style="text-align: justify;"> 7-4 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Novel Drug</a> Delivery Systems (NDDS)</p> <p style="text-align: justify;"> 7-5 Drug Excipient Compatibility Studies</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse8"> <span> Track 8 : </span>Quality Control & Assurance: </a> </h4> </div> <div id="collapse8" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 8.<strong><a href="https://pharmaceutics.cmesociety.com/about-us">Quality Control & Assurance:</a></strong></p> <p> Safeguard the integrity of <a href="https://pharmaceutics.cmesociety.com/abstract-submission">pharmaceutical</a> excellence. This session delves into the rigorous standards and analytical techniques that ensure product quality, safety, and compliance throughout the manufacturing process, fostering trust in every dose.</p> <p> 8-1Analytical techniques in QC</p> <p> 8-2 GMP compliance and audits</p> <p> 8-3 Quality assurance in <a href="https://pharmaceutics.cmesociety.com/registration">pharmaceutical</a> manufacturing</p> <p> 8-4 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Sterility Assurance</a> and Aseptic Processing</p> <p> 8-5Risk Management and Quality Systems</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse9"> <span> Track 9 : </span>Continuous Manufacturing & Process Innovation: </a> </h4> </div> <div id="collapse9" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 9.<a href="https://pharmaceutics.cmesociety.com/registration"><strong>Continuous Manufacturing & Process Innovation:</strong></a></p> <p> Revolutionize <a href="https://pharmaceutics.cmesociety.com/abstract-submission">pharmaceutical</a> production. This session explores the shift from traditional batch processing to continuous manufacturing, highlighting cutting-edge technologies that streamline production, enhance quality, and enable real-time process monitoring for increased efficiency and agility.</p> <p> 9-1 Implementing continuous manufacturing</p> <p> 9-2 Process analytical technology (PAT)</p> <p> 9-3 Real-time process monitoring</p> <p> 9-4 Machine Learning and <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Artificial Intelligence</a> in Process Optimization</p> <p> 9-5 Regulatory Considerations for Continuous Manufacturing</p> <p> <strong> </strong></p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse10"> <span> Track 10 : </span>Biologics & Biosimilars: </a> </h4> </div> <div id="collapse10" class="panel-collapse collapse "> <div class="panel-body"> <p><p> <strong>10.<a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Biologics & Biosimilars</a></strong><strong>:</strong></p> <p> Unlocking the potential of complex therapeutics. This session delves into the intricate world of biologics and biosimilars, exploring their development, manufacturing challenges, characterization, and regulatory pathways, ultimately increasing access to life-changing treatments</p> <p> 10-1 Biologics manufacturing challenges</p> <p> 10- 2 Biosimilar characterization</p> <p> 10-3 Biosimilar regulatory pathways</p> <p> 10-4 Immunogenicity and Safety of <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Biosimilars</a></p> <p> 10-5 Economic and Market Access Considerations for Biosimilars</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse11"> <span> Track 11 : </span>Pharmacokinetics (PK) & Pharmacodynamics (PD) </a> </h4> </div> <div id="collapse11" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 11.<a href="https://pharmaceutics.cmesociety.com/organizing-committee"><strong>Pharmacokinetics (PK) & Pharmacodynamics (PD</strong></a><strong>):</strong></p> <p style="text-align: justify;"> Decipher the complex interplay between <a href="https://pharmaceutics.cmesociety.com/about-us"> drug, </a> and body. This session unravels how medications are absorbed, distributed, metabolized, and eliminated (PK), and how they exert their <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">therapeutic</a> or adverse effects (PD), paving the way for optimized dosing and personalized medicine.</p> <p style="text-align: justify;"> 11-1 <a href="https://pharmaceutics.cmesociety.com/registration">PK/PD</a> modeling and simulation</p> <p style="text-align: justify;"> 11-2 <a href="https://pharmaceutics.cmesociety.com/registration">Drug metabolism</a> and transport</p> <p style="text-align: justify;"> 11-3 Drug Interactions and Adverse Reporting</p> <p style="text-align: justify;"> 11-4 Population PK/PD and Individualized Dosing</p> <p style="text-align: justify;"> 11-5PK/PD in Special Populations</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse12"> <span> Track 12 : </span>Drug Interactions & Adverse events: </a> </h4> </div> <div id="collapse12" class="panel-collapse collapse "> <div class="panel-body"> <p><p> <strong>12. </strong><a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Drug</strong> <strong>Interactions & Adverse events</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Master the intricate dance of medications within the body. This session unravels the complexities of <a href="https://pharmaceutics.cmesociety.com/registration">polypharmacy</a>, exploring how <a href="https://pharmaceutics.cmesociety.com/about-us"> drug, </a>interact, predicting potential <a href="https://pharmaceutics.cmesociety.com/registration">adverse events</a>, and equipping healthcare providers with strategies to optimize patient safety and minimize risks.</p> <p style="text-align: justify;"> 12-1 Predicting <a href="https://pharmaceutics.cmesociety.com/about-us"> </a>interactions</p> <p style="text-align: justify;"> 12-2 Adverse event reporting and management</p> <p style="text-align: justify;"> 12-3 <a href="https://pharmaceutics.cmesociety.com/registration">Pharmacovigilanc</a></p> <p style="text-align: justify;"> 12-4 Drug- Drug Interaction (DDI) Risk Assessment and Mitigation Strategies</p> <p style="text-align: justify;"> 12-5Patient-Specific Factors Influencing <a href="https://pharmaceutics.cmesociety.com/abstract-submission"> </a>Interactions and Adverse Events<strong> </strong></p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse13"> <span> Track 13 : </span>Special Populations: </a> </h4> </div> <div id="collapse13" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> <strong>13.<a href="https://pharmaceutics.cmesociety.com/organizing-committee">Special Populations:</a></strong></p> <p style="text-align: justify;"> This session dives into the nuances of <a href="https://pharmaceutics.cmesociety.com/about-us"> Global development, </a> therapy in pediatric, geriatric, and other special populations, addressing challenges and opportunities for optimizing <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">medication</a> safety and efficacy in these diverse patient groups.</p> <p style="text-align: justify;"> 13-1 Pediatric <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Pharmacology</a></p> <p style="text-align: justify;"> 13-2 Geriatric pharmacology</p> <p style="text-align: justify;"> 13-3 <a href="https://pharmaceutics.cmesociety.com/about-us">Drug </a>therapy in pregnancy</p> <p style="text-align: justify;"> 13-4 Therapy in Patients with Renal or Hepatic Impairment</p> <p style="text-align: justify;"> 13-5 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Pharmacogenomics</a> and Personalized Medicine in Special Populations</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse14"> <span> Track 14 : </span>Precision Medicine: </a> </h4> </div> <div id="collapse14" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 14.<a href="https://pharmaceutics.cmesociety.com/organizing-committee"><strong>Precision Medicine</strong></a><strong>:</strong></p> <p> Revolutionize <a href="https://pharmaceutics.cmesociety.com/registration">healthcare</a> with tailored treatments. This session explores the cutting-edge science of utilizing patients' genetic, environmental, and lifestyle data to create individualized therapies, maximizing effectiveness and minimizing side effects for optimal health outcomes.</p> <p> 14-1 <a href="https://pharmaceutics.cmesociety.com/registration">Pharmacogenomics</a> and personalized dosing,</p> <p> 14-2 Biomarker development and validation,</p> <p> 14-3 Companion diagnostics.</p> <p> 14-4 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Artificial Intelligence</a> and Machine Learning in Precision Medicine</p> <p> 14-5 Ethical and Regulatory Considerations in <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Precision Medicine</a></p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse15"> <span> Track 15 : </span>Rare Diseases & Orphan Drugs: </a> </h4> </div> <div id="collapse15" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> <strong>15. <a href="https://pharmaceutics.cmesociety.com/registration">Rare Diseases & Orphan Drugs:</a></strong></p> <p style="text-align: justify;"> Illuminating the path for underserved patients. This session explores the unique challenges and opportunities in developing treatments for rare diseases, navigating regulatory incentives, and fostering collaboration to bring hope to those affected by these conditions</p> <p style="text-align: justify;"> 15-1 Orphan drug design process</p> <p style="text-align: justify;"> 15-2 <a href="https://pharmaceutics.cmesociety.com/about-us">Clinical trial</a> challenges in rare diseases</p> <p style="text-align: justify;"> 15-3 Patient advocacy and access</p> <p style="text-align: justify;"> 15-4 Therapeutic Innovations for Rare Diseases: Accelerating Development & Improving Patient Outcomes</p> <p style="text-align: justify;"> 15-5 Global Perspectives on Rare Disease Research and Drug Development</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse16"> <span> Track 16 : </span> Drug Delivery Systems: </a> </h4> </div> <div id="collapse16" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 16 . <a href="https://pharmaceutics.cmesociety.com/venue-hospitality"><strong> Drug Delivery Systems:</strong></a></p> <p> Transforming <a href="https://pharmaceutics.cmesociety.com/about-us"> drug </a> delivery for optimized <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">therapeutic</a> outcomes. This session explores cutting-edge advancements, from nanoparticles and liposomes to controlled-release and targeted delivery, revolutionizing how medicines reach their destination and enhancing patient experiences</p> <p> 16-1 <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Nanoparticle</a> drug delivery</p> <p> 16-2 Liposomal formulations</p> <p> 16-3 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Targeted drug </a>delivery technologies</p> <p> 16-4 Oral Controlled Release Drug Delivery</p> <p> 16-5 Transdermal Drug Delivery Systems</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse17"> <span> Track 17 : </span>Digital Health & AI in Pharma: </a> </h4> </div> <div id="collapse17" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 17.<a href="https://pharmaceutics.cmesociety.com/organizing-committee"><strong>Digital Health & AI in Pharma</strong></a><strong>:</strong></p> <p style="text-align: justify;"> This session explores the transformative potential of artificial intelligence and digital technologies in <a href="https://pharmaceutics.cmesociety.com/about-us"> drug </a>discovery, <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">clinical trials</a>, personalized medicine, and patient care, paving the way for a new era of data-driven healthcare solutions.</p> <p style="text-align: justify;"> 17-1 AI in <a href="https://pharmaceutics.cmesociety.com/about-us">Drug </a>discovery</p> <p style="text-align: justify;"> 17-2 <a href="https://pharmaceutics.cmesociety.com/registration">Digital biomarkers</a> and patient monitoring</p> <p style="text-align: justify;"> 17-3 Real-world data and AI</p> <p style="text-align: justify;"> 17-4 Virtual clinical trials and Decentralized <a href="https://pharmaceutics.cmesociety.com/about-us">Research</a></p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse18"> <span> Track 18 : </span>3D Printing & Personalized Medicine: </a> </h4> </div> <div id="collapse18" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 18.<a href="https://pharmaceutics.cmesociety.com/call-for-abstracts"><strong>3D Printing & Personalized Medicine</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Transforming healthcare through customization. This session delves into the innovative use of 3D printing to create patient-specific medications, implants, and medical devices, revolutionizing treatment approaches and enhancing patient care.</p> <p style="text-align: justify;"> 18-1 3D printed <a href="https://pharmaceutics.cmesociety.com/about-us">drug</a> delivery systems</p> <p style="text-align: justify;"> 18-2 Personalized dosage forms</p> <p style="text-align: justify;"> 18-3 3D bio printing in regenerative <a href="https://pharmaceutics.cmesociety.com/abstract-submission">medicine</a></p> <p style="text-align: justify;"> 18-4 3D-Printed Prosthetics and Orthotics</p> <p style="text-align: justify;"> 18-5 3D-Printed Surgical Models and Guides</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse19"> <span> Track 19 : </span>Regenerative Medicine & Cell Therapies: </a> </h4> </div> <div id="collapse19" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 19. <a href="https://pharmaceutics.cmesociety.com/organizing-committee"><strong>Regenerative Medicine & Cell Therapies:</strong></a></p> <p style="text-align: justify;"> Igniting the body's healing potential. This session explores the frontiers of <a href="https://pharmaceutics.cmesociety.com/abstract-submission">regenerative medicine</a>, delving into cutting-edge cell therapies, tissue engineering, and gene therapies that hold the promise of repairing damaged tissues and organs, offering new hope for patients with chronic and debilitating conditions.</p> <p style="text-align: justify;"> 19-1 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Stem cell</a> therapies</p> <p style="text-align: justify;"> 19-2 <a href="https://pharmaceutics.cmesociety.com/about-us">Gene</a> therapy approaches</p> <p style="text-align: justify;"> 19-3 Ethical considerations in regenerative medicine</p> <p style="text-align: justify;"> 19-4 Tissue Engineering and Biomaterials</p> <p style="text-align: justify;"> 19-5 <a href="https://pharmaceutics.cmesociety.com/registration">Immunotherapy</a> and Immune Modulation in Regenerative Medicine</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse20"> <span> Track 20 : </span>Nanotechnology & Nano medicine: </a> </h4> </div> <div id="collapse20" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> <strong>20 <a href="https://pharmaceutics.cmesociety.com/about-us">Nanotechnology & Nano medicine:</a></strong></p> <p style="text-align: justify;"> Harnessing the power of the infinitesimal. This session explores the revolutionary applications of nanoscale materials and devices in medicine, from targeted <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts"> drug </a>delivery and diagnostics to regenerative therapies and innovative <a href="https://pharmaceutics.cmesociety.com/registration">medical imaging</a>, pushing the boundaries of healthcare innovation.</p> <p style="text-align: justify;"> 20-1 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Nanomaterial’s</a> for diagnostics</p> <p style="text-align: justify;"> 20-2 Therapeutic nanoparticles,</p> <p style="text-align: justify;"> 20-3 Nano medicine in <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">cancer therapy</a></p> <p style="text-align: justify;"> 20-4 Nanomedicine for Infectious Disease</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse21"> <span> Track 21 : </span>Regulatory Science & Policy </a> </h4> </div> <div id="collapse21" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 21. <a href="https://pharmaceutics.cmesociety.com/registration"><strong>Regulatory Science & Policy</strong></a></p> <p style="text-align: justify;"> Navigate the evolving landscape of <a href="https://pharmaceutics.cmesociety.com/about-us"> Global development, </a> regulation. This session explores cutting-edge regulatory science, policy trends, and global harmonization efforts to ensure patient safety while fostering innovation and accelerating access to life-changing therapies.</p> <p style="text-align: justify;"> 21-1 Evolving regulatory landscape</p> <p style="text-align: justify;"> 21-2 Patient-focused drug therapy</p> <p style="text-align: justify;"> 21-3 Regulatory harmonization efforts.</p> <p style="text-align: justify;"> 21-4 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Health Technology</a> Assessment (HTA) and Decision Making</p> <p style="text-align: justify;"> 21-5 Value-Based Pricing and Contracting</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse22"> <span> Track 22 : </span>Intellectual Property & Patent Law: </a> </h4> </div> <div id="collapse22" class="panel-collapse collapse "> <div class="panel-body"> <p><p> 22. <a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Intellectual Property & Patent Law:</strong></a></p> <p> <span style="text-align: justify;"> Exploring the intricate world of </span><a href="https://pharmaceutics.cmesociety.com/abstract-submission" style="text-align: justify;">pharmaceutical</a><span style="text-align: justify;"> innovation protection involves understanding various strategies for securing patents, defending intellectual property rights, and leveraging licensing agreements. This discussion covers the essentials for fostering a thriving environment for groundbreaking global development in </span><a href="https://pharmaceutics.cmesociety.com/abstract-submission" style="text-align: justify;">Pharma 2024</a><span style="text-align: justify;">.</span></p> <p style="text-align: justify;"> 22-1Patent strategies for <a href="https://pharmaceutics.cmesociety.com/abstract-submission">pharmaceuticals</a></p> <p style="text-align: justify;"> 22-2 Licensing and technology transfer</p> <p style="text-align: justify;"> 22-3 Bio similar patent litigation.</p> <p style="text-align: justify;"> 22-4 Data Exclusivity and Regulatory Data Protection</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse23"> <span> Track 23 : </span>Medical Affairs & Scientific Communication: </a> </h4> </div> <div id="collapse23" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 23.<a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Medical Affairs & Scientific Communication</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Elevate scientific discourse for impactful healthcare solutions. In the <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Pharma 2024 Conference</a> session, we explore strategies for effective scientific communication, fostering collaboration between medical affairs and <a href="https://pharmaceutics.cmesociety.com/about-us">healthcare professionals</a> to ensure that evidence-based insights shape clinical practice and improve patient outcomes.</p> <p style="text-align: justify;"> 23-1 Medical writing and publication</p> <p style="text-align: justify;"> 23-2 Scientific engagement with <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">healthcare professionals</a></p> <p style="text-align: justify;"> 23-3 Medical information management.</p> <p style="text-align: justify;"> 23-4 Evidence Generation and Real-World Data</p> <p style="text-align: justify;"> 23-5 Patient-Focused Communication and Advocacy</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse24"> <span> Track 24 : </span>. Ethical Considerations in Pharma: </a> </h4> </div> <div id="collapse24" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 24. <a href="https://pharmaceutics.cmesociety.com/about-us"><strong>Ethical Considerations in Pharma</strong></a><strong>:</strong></p> <p style="text-align: justify;"> Defining a responsible course in pharmaceutical innovation. In the <strong>Pharma 2024 Conference</strong> session, we explore the <strong>ethical complexities</strong> surrounding <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">drug development</a><strong>, </strong><strong>marketing, pricing</strong><strong>,</strong> and <strong>access</strong>, seeking to foster a <strong>transparent</strong> and <a href="https://pharmaceutics.cmesociety.com/abstract-submission">equitable healthcare</a> landscape that prioritizes <strong>patient well-being</strong> and <strong>societal benefit</strong>.</p> <p style="text-align: justify;"> 24-1 Research ethics in <a href="https://pharmaceutics.cmesociety.com/registration">clinical trials</a></p> <p style="text-align: justify;"> 24-2 Pricing and access to medicines</p> <p style="text-align: justify;"> 24-3 Ethical Marketing and Promotion of <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a>s</p> <p style="text-align: justify;"> 24-4 Ethical Considerations in Global Health and Access to Medicines</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse25"> <span> Track 25 : </span>Real-World Evidence (RWE) & Post-Market Surveillance: </a> </h4> </div> <div id="collapse25" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 25. <strong><a href="https://pharmaceutics.cmesociety.com/abstract-submission">Real-World Evidence (RWE) & Post-Market Surveillance</a></strong>:</p> <p style="text-align: justify;"> In the <a href="https://pharmaceutics.cmesociety.com/registration">Pharma 2024 Conference</a> session, we explore the growing importance of <strong>real-world evidence</strong> (data collected outside of traditional clinical trials) in evaluating <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">drug safety</a> and <strong>effectiveness</strong> in real-world settings. It also covers the role of <strong>post-market surveillance</strong> in identifying and mitigating risks associated with marketed drugs.</p> <p style="text-align: justify;"> 25-1 RWE study <a href="https://pharmaceutics.cmesociety.com/about-us">design </a>and methodology</p> <p style="text-align: justify;"> 25-2 Integrating RWE with clinical trial data</p> <p style="text-align: justify;"> 25-3 Post-market safety monitoring and <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmacovigilanc</a></p> <p style="text-align: justify;"> 25-4 RWE in regulatory decision-making</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse26"> <span> Track 26 : </span>Drug Repurposing & Drug Combinations: </a> </h4> </div> <div id="collapse26" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> <strong>26. </strong><a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Drug</strong></a> <a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Repurposing</strong></a><strong> & </strong><a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Drug</strong></a> <a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Combinations</strong></a><strong>:</strong></p> <p style="text-align: justify;"> That session in the <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Pharma 2024</a> focuses on innovative approaches to drug combinations, including repurposing existing drugs for new indications and exploring the potential of these combinations to improve <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">therapeutic</a> outcomes.</p> <p style="text-align: justify;"> 26-1 Rational drug design combination</p> <p style="text-align: justify;"> 26-2 <a href="https://pharmaceutics.cmesociety.com/registration">clinical trials</a> for drug designs</p> <p style="text-align: justify;"> 26-3 Regulatory considerations for <a href="https://pharmaceutics.cmesociety.com/about-us">drug, </a> repurposing and combinations</p> <p style="text-align: justify;"> 26-4 Repurposing Drug Identifying New Uses for Old Medications</p> <p style="text-align: justify;"> 26-5 Combination Therapies: Optimizing <a href="https://pharmaceutics.cmesociety.com/about-us">Drug</a> Efficacy and Safety through Synergy</p> <p> </p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse27"> <span> Track 27 : </span>. Pharmaceutical Microbiology & Sterility Assurance: </a> </h4> </div> <div id="collapse27" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 27. <a href="https://pharmaceutics.cmesociety.com/registration"><strong>Pharmaceutical</strong><strong> Microbiology & Sterility Assurance</strong></a><strong>:</strong></p> <p style="text-align: justify;"> <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">Pharma 2024</a> will feature a presentation examining the pivotal role of microbiological principles in <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Pharma manufacturing</a> and quality control, underscoring the necessity of sterility assurance to prevent contamination and safeguard <a href="https://pharmaceutics.cmesociety.com/registration">patient safety</a>..</p> <p style="text-align: justify;"> 27-1 Microbiological contamination control strategies</p> <p style="text-align: justify;"> 27-2 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Sterilization</a> methods and validation</p> <p style="text-align: justify;"> 27-3 Environmental monitoring programs</p> <p style="text-align: justify;"> 27-4 Microbial risk assessment and <a href="https://pharmaceutics.cmesociety.com/about-us">mitigation</a></p> <p style="text-align: justify;"> </p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse28"> <span> Track 28 : </span> Pharmaceutical Packaging & Labeling: </a> </h4> </div> <div id="collapse28" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 28. <a href="https://pharmaceutics.cmesociety.com/abstract-submission"><strong>Pharmaceutical</strong><strong> Packaging & Labeling:</strong></a></p> <p style="text-align: justify;"> This session addresses the latest developments in <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a> packaging and labeling technologies, focusing on their role in protecting drug products, ensuring product integrity, and providing essential information to patients and <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">healthcare professionals</a>.</p> <p style="text-align: justify;"> 28-1 <a href="https://pharmaceutics.cmesociety.com/abstract-submission">Pharma Innovative</a> packaging materials and designs</p> <p style="text-align: justify;"> 28-2 Smart packaging and anti-counterfeiting measures</p> <p style="text-align: justify;"> 28-3 Labeling regulations and compliance</p> <p style="text-align: justify;"> 28-4 <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Patient-centric</a> packaging design</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse29"> <span> Track 29 : </span> Global Health & Access to Medicines </a> </h4> </div> <div id="collapse29" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> 29. <a href="https://pharmaceutics.cmesociety.com/organizing-committee"><strong>Global Health & Access to Medicines:</strong></a></p> <p style="text-align: justify;"> The Pharma 2024 Conference will include a forum that examines the challenges and opportunities in ensuring equitable access to <a href="https://pharmaceutics.cmesociety.com/about-us">medicines</a> in low- and middle-income countries, addressing issues such as <a href="https://pharmaceutics.cmesociety.com/abstract-submission">affordability</a>, intellectual property rights, and regulatory barriers. </p> <p style="text-align: justify;"> 29-1 <a href="https://pharmaceutics.cmesociety.com/registration">Global health</a> disparities and the need for access to medicines</p> <p style="text-align: justify;"> 29-2 Pricing and reimbursement strategies</p> <p style="text-align: justify;"> 29-3 Intellectual property rights and access to <a href="https://pharmaceutics.cmesociety.com/about-us">medicines</a></p> <p style="text-align: justify;"> 29-4 Local Manufacturing and Technology Transfer</p> <p style="text-align: justify;"> 29-5 Public-Private Partnerships (PPPs) for Global Health</p> </p> <ul> </ul> </div> </div> </div> <div class="panel panel-default"> <div class="panel-heading"> <h4 class="panel-title"> <a class="accordion-toggle" data-toggle="collapse" href="#collapse30"> <span> Track 30 : </span> Case Studies and Reports </a> </h4> </div> <div id="collapse30" class="panel-collapse collapse "> <div class="panel-body"> <p><p style="text-align: justify;"> <strong>30. </strong><a href="https://pharmaceutics.cmesociety.com/call-for-abstracts"><strong>Case Studies and Reports:</strong></a></p> <p style="text-align: justify;"> Case studies and reports in the <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a> industry act as a compass, guiding stakeholders through the complex landscape of <a href="https://pharmaceutics.cmesociety.com/about-us">drug</a> development and healthcare delivery. They provide a firsthand account of impacts and setbacks, offering actionable insights and lessons learned that can shape future strategies, policies, and ultimately, improve <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">patient</a> outcomes.</p> <p style="text-align: justify;"> 30-1 Drug Discovery & Development</p> <p style="text-align: justify;"> 30-2 <a href="https://pharmaceutics.cmesociety.com/call-for-abstracts">pharmaceutical</a> Chemistry & Manufacturing</p> <p style="text-align: justify;"> 30-3 <a href="https://pharmaceutics.cmesociety.com/venue-hospitality">Clinical Pharmacology</a><strong> & Therapeutics</strong></p> <p style="text-align: justify;"> 30-4 Regulatory Affairs & Market Access</p> <p style="text-align: justify;"> 30-5 Real-World Evidence & Post-Market Surveillance</p> </p> <ul> </ul> </div> </div> </div> </div> </div> <div class="col-md-3"> <aside> <div class="thumbnail border border-info text-center schedule"> <p class="clearfix"><i class="fa 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