Courses

Explore the fundamentals of clinical research in this informative 58-minute webinar co-hosted by Immunovant, The Center for Information and Study on Clinical Research Participation, Inc. (@CISCRP615), and the Graves' Disease & Thyroid Foundation (GDATF). Presented by Bridget Chapital, MEd, Advisory Board Member of CISCRP and Founder of Hypothesis Haven Science Club, the webinar delves into key aspects of clinical studies. Learn from expert insights as Jaye Bea Smalley, Head of Patient Advocacy at Immunovant, hosts the session, with Kimberly Dorris, Executive Director of GDATF, moderating the discussion. Gain valuable knowledge about the clinical research process, its importance in advancing medical treatments, and how it impacts patients with Graves' disease and thyroid conditions. Access additional resources on clinical trials through the GDATF website for a comprehensive understanding of this crucial aspect of medical advancement.

Explore the transformation of clinical research through modern platform engineering in this 19-minute conference talk from Conf42 Platform Engineering 2025. Learn how to address the significant challenges facing traditional clinical research processes and discover a comprehensive vision for modernizing research infrastructure. Examine the strategic benefits of implementing low-code platforms in clinical environments and analyze a detailed case study demonstrating successful transformation through low-code solutions. Dive into the technical implementation aspects of building robust clinical research platforms while understanding the critical human factors that influence platform adoption and user engagement. Review measurable business outcomes that demonstrate the value of platform engineering investments in clinical research settings. Investigate emerging trends shaping the future of clinical research technology and understand the shift toward patient-centric research platforms that prioritize user experience and accessibility. Gain insights into best practices for building scalable, efficient clinical research infrastructure that can adapt to evolving regulatory requirements and research methodologies.

This Clinical Research: Help and Review course is the simplest way to master clinical research concepts and practices. Review short and fun videos focusing on clinical study processes, clinical trials and data research. Practice quizzes help to ensure your full understanding of this material.

Complete, Certified ICH GCP E6 (R3) Course for Investigators, Study Coordinators, Sponsors, Monitors and Study staff What you'll learn: Identify and understand the ICH-GCP requirements throughout the conduct of clinical trialsLearn the core principles of ICH-GCP R3 and how to implement them in practiceDefine the roles and responsibilities of each involved key stakeholder: Ethics Committees, Sponsors and InvestigatorsUnderstand the purpose of the essential documents and the best practice for filing in the TMFUnderstand the essential requirements and contents of the Investigator's Brochure and the ProtocolPractice on real cases: Identify common ICH-GCP inspection findings (FDA warning letters) and how to avoid themPractice on real cases: Conduct a gap analysis in your organization based on a real MHRA inspection report Welcome to the only up-to-date, complete edition of the ICH GCP course!This course meets the Minimum Criteria for ICH E6 GCP Investigator and Site Personnel Training that TransCelerate has identified as necessary to enable mutual recognition of GCP training.This course offers the first professional, fundamental on-line ICH GCP detailed course for Investigators, Study Coordinators, Sponsors, Clinical Project Managers, Monitors and any other Clinical Study staff requiring knowledge in GCP for a successful execution your clinical trials.My name is Dr. Vincent Baeyens PhD, Ihave more than 20 years of experience in running Clinical Trials in Global and mid-size Pharma, and Biotech settings. I have worked with most of the Global as well as several niche CROs andI am also an expert inCRO Management and Oversight, budgeting and Risk Management. In this course, you will be able to understand based on my experience the key ICH GCPrequirements to design, conduct, record and report clinical trials in humans from A to Z. We will review the role and responsibilities of the key stakeholders and the structure of the essentials documents.To facilitate the learning of beginner students, the course has been broken up on purpose in several small lectures.Note: If you are a more advanced student, you can increase the speed of lecture to learn the course at your own pace.This course will provide you with a strong support to prepare for successful regulatory ICH GCP inspections and audits.I will lead you step-by-step through the ICH GCPE6, and you will learn & understand: What is GCP and why GCP is important in clinical researchThe link between the Declaration of Helsinki and current GCPThe definition of the key definitions of terms and concepts used in clinical research, including stakeholders involved and essential documentsThe ICH GCP Principles of Revision 2 and Revision 3 and practical advices to apply them in your clinical trialsThe responsibilities of ethics committees, its composition, function, operational aspects and obligationsThe detailed responsibilities of the Investigator throughout the trial, including his/her qualifications, compliance to protocol, communication with Ethics Committees, safety reporting, and final reportingHow to write an adequate Protocol / protocol amendment and rationale for its structureThe What, the Why and the How for an effective writing of the Investigator's BrochureThe purpose of Essential Documents in clinical research: How and Where to file them in the Trial Master File (TMF)The common ICH GCP audit and inspection findings in clinical trials with practical exercises (FDA, MHRA) Iwill illustrate the GCP concepts with several practical tips & tricks , so that you will be able to apply ICH GCP to your daily practice from Day 1!Quizzes are proposed to test your knowledge along your journey. A final Quiz at the end of the course will consolidate your knowledge.Feel free to look at the content of the course to know more and contact me any time if you have any questions!After the course, spend 1 hour with the EXPERT to answer ALLthe questions that you would have!! All you have to do is to send me an e-mail with your questions and contact details, and I will set up a call with you.I am of course available personally during the course as well to answer your questions or comments! I am looking forward to seeing you inside the course! Sincerely, Vincent---Updates:July 2025: Updated with ICH-GCP(R3)guidelineJune 2024: Added ICH-GCP(R3) Annex 2concept paperJanuary 2024: Updated Bonus section; added the ICH-GCP(R3) Overview of comments received on Step 2. Comments will now be sent to the ICH E6 (R3) Expert Working Group for consideration in the context of Step 3 of the ICH process.September 2023: Updated section of ICHGCPR3Draft Principles and added resource documentationAugust 2023: Added list of Acronyms and Abbreviations used in the course (section 1)June 2023: Added DRAFTICH GCP(R3) Annexe 1 (interventional clinical trials), its summary of changes and explanatory video in the resources. This version is made available by the ICH for public consultation until September 2023 (step 2 of the ICH process)May 2023: Added link to ICH E8 (R1) in resources of quality managementFebruary 2023: Added awareness of the most common GCP findings (lecture 4)January 2023: Edited English subtitles, adding French subtitlesDecember 2022: Added assignment: Practical risk assessment based on UK MHRA inspection report (section 11)October 2022: Added assignment: Practical exercises from real FDA inspection cases (section 10)September 2022: Added updates on ongoing development of Revision 3 of ICH-GCP (section 12)

Explore emerging trends in clinical research and gain insights into the future of pediatric critical care medicine in this 23-minute podcast featuring Dr. Robert Tasker, Editor-in-Chief of Pediatric Critical Care Medicine Journal. Learn to forecast research trends using current data, understand factors considered by editors when selecting content submissions, and boost confidence in submitting work to journals. Delve into topics such as biomarkers for pediatric septic shock, machine learning models in cardiac ICUs, COVID-19's impact on PICUs, and neurologic manifestations in children. Discover tips for improving manuscript submissions and increasing publication chances. Access referenced articles covering various aspects of pediatric critical care, from rehabilitation prevalence to structured clinical research report writing.

Certification on ICH GCP E6 R2 Good Clinical Practice for Clinical Research The Only Complete Course You Can Find Online What you'll learn: What Good Clinical Practices Are?Guidelines of What An Ethical And Safe Trail Is?The Rights And Importance Of Consent Of The Trial SubjectsThe Duties Of The Sponsor And Investigator Of The TrialWhat Is International Council For Harmonization?Aims Of ICHHow Was ICH Established?The Importance Of ICHGroups Working Within ICHICH GCP E6 R2 Efficacy GuidelinesLink Between ICH And GCPAll About The Institutional Review Board, Investigators, Sponsors, Clinical Trial Protocol And Protocol Amendment, Investigator’s Brochure, Essential Documents ***Why this course is considered as a TOP RATED and BEST SELLING course for the ICH GCP category on Udemy?***See what students are talking about in this course:5***** Star RatingI’m very glad I enrolled in this class! There’s so much information to be absorbed and she did a great job in presenting everything in as much detail as possible, but at the same time simplifying it to make your learning experience a lot smoother. This is a great course if you’re just starting out and want to know the fundamentals of GCP. This master class has it all! ---Devon Roman5***** Star RatingShe is a great instructor, very transparent, cuts out all the BS getting straight to the meat and potatoes of the subject at hand, exactly how I like to learn.I am happy about investing in this course. The videos are over the shoulder at the right pace explaining the process of understanding the clauses.The course has left me feeling confident that I can achieve my goals, plus I had so much fun learning.If you create any more courses, you have a repeat customer in me.--- Rebecca5***** Star RatingVery well constructed course covering all the topics I was interested in. Really liked the step-by-step approach and tasks broken into manageable chunks, allowing me to absorb the information. The tutor was great, the notes were very helpful and I made a lot of use of the Quizzes and Assignments section.Highly recommend the course for either a beginner or someone with some experience but a bit rusty (such as me).--- Reshma 5***** Star RatingShe is an amazing teacher, the best I could find so far. She is knowledgeable, explains very well, has a nice and soothing voice, and has a great sense of presentation.The course is also more hands-on than a lot of other courses where you practically just watch guys read. She explains clauses practically who ICH GCP E6 document.If you want to learn and understand GCP or clinical research in general, this is a great place to start.--- Varun P5***** Star RatingThis is an excellent, cost-effective, and comprehensive course and I'm so glad to enroll in the class. Plus, I've learned so much from the basics that have been taught. I'm so grateful to have the instructor spending time to develop this course and share knowledge. Again, thanks, and this course is highly recommended!--- Dennis Clayton5***** Star RatingThe content was helpful and this was a nice quick review.--- Ayesha A. Rizvi, Ed.D.5***** Star RatingThe information is explained in a detailed manner--- Monique Brown5***** Star RatingBravo--- Tshering JAMTSHO--------------------------------------------------------------------------------------------COMPLETE COURSE DESCRIPTION:Welcome to the complete ICH Good Clinical Practices E6 R2 course.In this course, we will learn what Good clinical practices are, guidelines of what an ethical and safe trial is, the rights and importance of consent of the trial subjects, the duties of the sponsor and investigator of the trial, and much more. Basically, I will walk you through the entire GCP guidelines document step by step.My name is Warda Naz, and I will be leading you through this course.Here at Magine Solutions highly experienced instructors, engineers, and doctors with more than 10 years of experience in the industry will guide you through very high-quality online courses.At the end of the course, you will be able to understandWhat is International Council for harmonization?Aims of ICHHow was ICH established?The importance of ICH.Groups working within ICHEfficacy GuidelinesWhat are Good clinical Practices (GCP)?The link between ICH and GCPAll about the Institutional review board, investigators, sponsors, clinical trial protocol and protocol amendment, investigator’s brochure, essential documents for the conduct of a clinical trial, and much more.We will also learn to understand these concepts by looking at case studies to strengthen the theoretical concepts.The ideal student for this course is anyone who wants to learn about the ICH GCP E6 document or an existing professional who wants to expand on their current skills. There are no requirements necessary to enroll. I only ask to come open-minded and ready to learn.Feel free to take a look at the course description and I look forward to seeing you inside. Thank you!!--------------------------------------------------------------------------------------------

Explore the world of clinical research and trials in this 25-minute grand rounds presentation by Dr. David Moore, a neurologist from McFarland Clinic. Gain insights into the various phases of clinical research, from discovery to preclinical testing and clinical studies. Learn about the role of Accellacare in facilitating trials, including recent COVID-19 treatment studies. Understand the involvement of investigators, study coordinators, and the importance of clinical practice training. Discover the process of investigative reimbursement and get a glimpse of the research pipeline. Conclude with a Q&A session to address any lingering questions about this crucial aspect of medical advancement.

Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course, you will explore clinical research – its challenges and its huge benefits to modern healthcare. You will work through case studies and examine how research contributes to the treatment of major diseases, such as cancer and dementia, examining the process of conducting research and the ethical questions raised. You will learn how members of a research team, academics and participants in clinical research all contribute to this process of discovery. This course has been ranked as one of the best online courses of all time by online course aggregator class central. This course is designed for anyone who wants to know more about modern healthcare, and the role of clinical research and discovery within it. It will be of special interest to: students at school or college; undergraduates or postgraduates who are contemplating a career in healthcare or the life sciences; and health and social care professionals and practitioners who want to find out more about the role of clinical research in improving healthcare. This course has been certified by the CPD Certification Service as conforming to continuing professional development principles. By completing the course you will have achieved 16 hours of CPD time. No previous knowledge is needed to take this course.

This course presents critical concepts and practical methods to support planning, collection, storage, and dissemination of data in clinical research. Understanding and implementing solid data management principles is critical for any scientific domain. Regardless of your current (or anticipated) role in the research enterprise, a strong working knowledge and skill set in data management principles and practice will increase your productivity and improve your science. Our goal is to use these modules to help you learn and practice this skill set. This course assumes very little current knowledge of technology other than how to operate a web browser. We will focus on practical lessons, short quizzes, and hands-on exercises as we explore together best practices for data management.

Complete Certified Course on Implementing and Applying mandatory CTR for EU and non-EU Clinical Research Professionals What you'll learn: Gain an overview of the Clinical Trial Regulation (CTR) to conduct trials in the EUUnderstand why changes to the Directive 2001/20/EC were madeLearn and understand the timeline for CTR introduction and transition periodLearn the essential definitions of terms under the CTRUnderstand how the Clinical Trial Information System (CTIS) is set upUnderstand the submission process of clinical trialsUnderstand the validation, assessment and decisions process of clinical trials under the CTRLearn the process to submit a Substantial Modification of the protocolLearn the process to submit a new Member State in an ongoing studyIdentify the safety and other reporting obligationsGrasp the risks and challenges associated with the CTR in sponsor organizationsPractical exercise: Conduct a risk assessment of a regulatory submission with the CTRPractical exercise: Planning a regulatory submission in line with the CTR Updates:[October 2025]: Lecture 15: Q&A Log updated, Walk in Clinic EMAlink added[November 2024]: Lecture 2: Updated key facts[January 2024]: Lecture 14 - CTIS Training material catalogue updated with latest information[March 2023]: Training document material from EMA updated and lecture 14 updated accordingly; New Q&A document from the CTIS/CTR query management working group attached (lecture 15)---On 31st January 2023, the Clinical Trial Regulation (CTR) 536/2014 came into force in the European Union (EU) and repealed the Clinical Trials Directive 2001/20/EC. With this Regulation, the EU harmonises the procedures for carrying out clinical trials across the EU states and simplifies the clinical trial approval process through a Clinical Trials Information System (CTIS).This course provides clinical research professionals in Sponsor and CROorganizations as well as investigational sites and study staff with an essential understanding of the CTR to help implement and comply with it.The programme highlights the most important of these key requirements and how these are impacting all EU as well as non-EU sponsors conducting clinical trials in the EU.My name is Dr. Vincent Baeyens PhD, Ihave more than 20 years of experience in running Clinical Trials in Global and mid-size Pharma and Biotech settings.Benefits of attending this course include:Gain an overview of the Clinical Trial Regulation (CTR) to conduct trials in the EUUnderstand why changes to the Directive 2001/20/EC were madeLearn and understand the timeline for CTR introduction and transition periodLearn the essential definitions of terms under the CTRUnderstand how the Clinical Trials Information System (CTIS) is set upUnderstand the submission process of clinical trials in the CTISUnderstand the validation, assessment and decisions process of clinical trials under the CTRLearn the process to submit a Substantial Modification of the protocolLearn the process to submit a new Member State in an ongoing studyIdentify the safety and other reporting obligationsGrasp the risks and challenges associated with the CTR in sponsor organizationsPrepare a high-level submission planning under CTRQuizzes and assignments are proposed along your journey to test your knowledge.To facilitate the learning of beginner students, the course has been broken up on purpose in small lectures. If you are a more advanced student, you can increase the speed of lecture to learn the course at your desired pace.Important remark: Please note that this course does not go into the technicalities of the CTIS. References to adequate resources on the topic are provided.Feel free to look at the content of the course to know more and contact me any time if you have any questions!I am looking forward to seeing you inside the course!Sincerely,Vincent

Learn about advanced cell sorting techniques and their critical applications in clinical immunology research through this hour-long webinar presented by Dr. Luis M. Allende, Head of Cellular Immunology and Immunodeficiencies at University 12 de Octubre Hospital. Explore how cell sorting and DNA sequencing are essential for diagnosing somatic autoimmune lymphoproliferative syndrome (ALPS) and understanding inborn errors of immunity (IEI). Discover the role of cell sorting in identifying somatic variants and molecular characterization of diseases like Large Granular Lymphocyte Leukemia (LGLL). Gain insights into how these techniques contribute to studying mutations in genes like STAT3, STAT5B, and TET2, leading to better understanding of disease pathophysiology and personalized immunosuppression treatments. Master the latest developments in molecular variant analysis and their implications for both T-cell and NK-cell disorders in clinical immunology.

If you’ve ever skipped over the results section of a medical paper because terms like “confidence interval” or “p-value” go over your head, then you’re in the right place. You may be a clinical practitioner reading research articles to keep up-to-date with developments in your field or a medical student wondering how to approach your own research. Greater confidence in understanding statistical analysis and the results can benefit both working professionals and those undertaking research themselves. If you are simply interested in properly understanding the published literature or if you are embarking on conducting your own research, this course is your first step. It offers an easy entry into interpreting common statistical concepts without getting into nitty-gritty mathematical formulae. To be able to interpret and understand these concepts is the best way to start your journey into the world of clinical literature. That’s where this course comes in - so let’s get started! The course is free to enroll and take. You will be offered the option of purchasing a certificate of completion which you become eligible for, if you successfully complete the course requirements. This can be an excellent way of staying motivated! Financial Aid is also available.

Master clinical trial phases, ICH-GCP, key roles & protocol design—plus AI, RWE, and patient-centric innovations. What you'll learn: New Update (August-2025): Landing a Job in Clinical Research: CV, Interview, LinkedIn & Career TipsDesigned like top university programs—practical, structured, and podcast-style for real-world clinical research success.Define the roles and responsibilities of sponsors, CROs, CRAs, and site staff in clinical trials.Learn clinical research in podcast style — flexible, clear, and career-focused.Build a career roadmap and prepare for roles like CTA, CRA, CDM, and Clinical Project Manager.Bunes1: How to use EDC SystemBunes2: What's the Data Management Plan(DMP)Navigate all phases of a clinical trial, from study start-up through close-out and post-marketing.Busy schedule? No problem. Learn anywhere with our podcast-style format.Design and interpret clinical trial protocols, case report forms, and informed consent documents.Identify, document, and report Serious Adverse Events (SAEs) and apply pharmacovigilance practices.Apply digital tools, AI, and remote technologies in decentralized and modern clinical trial models.Evaluate real-world data (RWD) and real-world evidence (RWE) for regulatory and scientific decisions.Develop inclusive, patient-centric trial strategies that enhance recruitment and retention.Gain leadership insights to manage clinical operations and stakeholders strategically.Pair this course with our best-selling CDM course: link below:https://www.udemy.com/course/a-deep-dive-into-clinical-data-management-basics-to-advance/?referralCode=171061DA95F06F098379Create and manage Trial Master File (TMF) components with audit readiness and regulatory compliance in mind.Understand stakeholder alignment across sites, CROs, sponsors, and regulatory bodies.Apply risk-based monitoring and quality management techniques throughout clinical trials.Explore post-market safety surveillance and the role of Phase IV studies in long-term data collection.Clinical trials made simple — step-by-step, audio-first, and job-ready.Build your research career with engaging audio lessons and practical tools.Clinical research made modern — learn by listening, grow by doing. A Deep Dive into Clinical Research: Step-by-Step CertificateMaster trial phases, protocols, ethics, pharmacovigilance, and data operations in clinical research—step by step.Designed like top university programs—practical, structured, and podcast-style for real-world clinical research success. Whether you're a nurse, pharmacist, medical graduate, biologist, or life science student looking to break into clinical trials, this course is built for you.This comprehensive certificate program takes you through every essential part of the clinical trial process—from the foundational principles of Good Clinical Practice (GCP) to the execution of complex global studies. We’ll guide you through the roles of sponsors, CROs, CRAs, data managers, and regulators, while showing you how to design protocols, handle adverse events, and manage clinical data accurately.Why Enroll?Structured and practical, aligned with real-world clinical operationsPodcast-style delivery—perfect for flexible learningIncludes modern trends like AI applications in research and RWE integrationCertificate of completion for professional growthPodcast-style delivery for flexible, learner-friendly accessBuilt to meet Udemy Business quality and relevance standards What You’ll LearnClinical trial phases (I–IV) and their objectivesStudy protocols, regulatory compliance, and ICH-GCPRoles of Sponsors, CROs, CRAs, CRCs, and Regulatory AuthoritiesSerious Adverse Event (SAE) reporting and pharmacovigilanceDigital health tools, AI in trial optimization, and Real-World Evidence (RWE)Patient-centric trial design and future-ready methodologies You’ll also gain leadership insight, resume tools, and access to our downloadable resource kit to accelerate your career in clinical research.Already enrolled in our best-selling Clinical Data Management course? This is the perfect companion. Explore the CDM course

Explore the cutting-edge applications of artificial intelligence and machine learning in healthcare through this 51-minute lecture by Dr. Curtis Lisle from KnowledgeVis at the University of Central Florida. Discover how AI and ML technologies are revolutionizing both pre-clinical research and clinical healthcare applications, examining current research developments, implementation challenges, and future opportunities in medical data analysis, diagnostic tools, treatment optimization, and patient care systems. Learn about the practical considerations for integrating these advanced technologies into healthcare workflows and understand the potential impact on improving patient outcomes and medical research efficiency.

Explore the clinical applications of cytokine testing in this 40-minute webinar presented by Thomas Martin, a senior-level research scientist at ARUP Laboratories. Delve into the role of cytokines as the hormones of the immune system and their significance in cell signaling, host immune responses, and various physiological processes. Discover how cytokine testing, primarily used in research, is gaining clinical utility for monitoring immunomodulating therapies, ensuring safety in clinical trials, and managing cytokine storm syndrome. Learn about the challenges and potential of cytokine testing in diagnosing and understanding immune, infectious, allergic, and inflammatory disorders. Gain insights from Martin's expertise in laboratory medicine and biomedical sciences as he discusses the evolving landscape of cytokine testing beyond its traditional research applications.

Explore the ethical complexities of conducting clinical research in neonatal intensive care units in this 21-minute video lecture by Dr. Benjamin Wilfond, Director at the Treuman Katz Center for Pediatric Bioethics at Seattle Children's Hospital. Delve into the importance of research standardization, the process of obtaining informed consent, and the eight ethical benchmarks crucial for clinical research. Examine the contexts of randomized clinical trials and their real-world applications in neonatal care. Gain valuable insights into the unique challenges faced by researchers and healthcare professionals when studying vulnerable newborn populations. Originally published on September 19, 2019, this educational content is part of OPENPediatrics, an interactive digital learning platform sponsored by Boston Children's Hospital in collaboration with the World Federation of Pediatric Intensive and Critical Care Societies.

Hone data management skills to advance clinical research – and your career Effective data management in clinical trials is the backbone of credible research. Without it, we risk overlooking impactful discoveries and compromising the integrity of groundbreaking innovations. Hone one of medical research’s most important skills on this two-week, online course from the University of Birmingham. On this comprehensive deep dive of data management, you’ll explore how to handle trial data, from collection to archiving, and the quality processes required along the way. By the end, you’ll be able to design and implement robust data management plans to enhance the accuracy and reliability of your trial results, ultimately strengthening your team’s ability to deliver high-quality, impactful research. Grow as a data manager with critical management skills and data validation techniques On the first week of this course, you’ll lay the foundations for effective data management. Learn to create comprehensive data management plans and discover various validation strategies to ensure data accuracy. Promote quality assurance in clinical data management By the second week of this course, you’ll segue into the role of data collection and quality assurance. You’ll examine various monitoring strategies, including site and central monitoring, to maintain data integrity throughout the trial. You’ll then wrap up this course by understanding end-of-trial processes, including cleaning and archiving data. Learn with the experts at the University of Birmingham The University of Birmingham’s Centre for Clinical Trials is a leading UK institution for clinical trial research. With the help of their experts, who’ve crafted this course to deliver exclusive insights and in-demand skills, you’ll be supported throughout your learning journey. This introductory course is for anyone setting up clinical trials and responsible for ensuring trial data integrity, such as aspiring chief investigators, trial coordinators, managers, data managers, and administrators. No prior knowledge is needed to join.

Watch a comprehensive webinar on ANCA-Associated Vasculitis presented by nephrology expert Dr. Balazs Odler, PhD from the Medical University of Graz, Austria. Hosted by the EFIM Young Internists Section and moderated by Dr. Sina Karimi (Belgium) and Dr. Charlotte Keyser (Netherlands), this recorded session from November 27, 2024, delivers an inspiring and informative lecture on this important medical topic.

Explore the Vaccine Research Center's work through a comprehensive lecture by Camille Lange, part of the NIH Clinical and Translational Research Summer Course. Gain insights into vaccine development, cutting-edge research, and the center's role in combating infectious diseases. Learn about unique NIH resources, connect with researchers and program administrators, and discover potential career opportunities at the National Institutes of Health. This 28-minute presentation offers valuable knowledge for those interested in clinical and translational research, immunology, and vaccine science. For further information or questions about the course, contact the coordinator at odpcp@mail.nih.gov.

Overview of Marketing Research. Get free SMstudy® Certified Marketing Research Associate Certification with this course. What you'll learn: Gain a basic understanding of Marketing ResearchLearn the key concepts of Marketing Reserach This course contains anoverview of Marketing Research and is based on theSMstudy®Guide. It has 35high quality videos on Marketing Research including a brief about a brief history of Marketing Research. Upon completion of this course, students can get free 'SMstudy®Certified Marketing Research Associate' certification from . The course also touches upon the benefits of SMstudy®Guide. TheSMstudy®Guideis developed by VMEdu, Inc., a global certification course provider that has educated over 400,000 students world-wide in more than 3,500 companies. It explains Sales and Marketing concepts through a practical, process-oriented approach. Marketing Research, provides a framework for conducting Marketing Research for a company’s products, services, and brands. Marketing Researchis the systematic process of collecting, processing, and analyzing data to provide required information to decision makers. Marketing Research is linked to all other Aspects of Marketing as it provides critical insights that inform key decisions in all other marketing planning and strategies. The processes associated with planning and executing a marketing research project include understanding the research problem; deciding a suitable research design; collecting, processing, and analyzing data required to solve the problem; interpreting data; and presenting the findings/recommendations of the research project to the key decision makers.