Courses

Explore a thought-provoking video lecture examining the future of academic funding and its potential decline in the coming decades. Analyze the inefficiencies of academia's planned economy structure and evaluate five common arguments supporting the current academic system. Learn why these traditional justifications - including long-term research benefits, serendipitous discoveries, non-profit nature, expert requirements, and historical achievements - may not hold up under scrutiny. Delve into the underlying systemic issues within academia and consider predictions about its future transformation. The 22-minute analysis breaks down complex topics into digestible segments, from the fundamental problems facing modern academia to a detailed examination of its structural challenges and potential outcomes.

Climate Change and Global Affairs: Navigating a Warming World is a three-course specialization created by the Council on Foreign Relations. By completing this self-guided series, you will understand the natural and human causes of climate change and how climate change affects society and global affairs. You will also learn about the many approaches to mitigate and adapt to climate change’s effects and assess how governments can address climate change at the local, national, and international levels. In short, you will achieve climate literacy. Intended for all learners, this specialization may be of particular interest to: Social and environmental science educators (K-12, Higher Ed, Adult Learning, and Vocational Trainers) High school and college students interested in social and environmental science education Individuals preparing for existing and emerging climate-related careers Individuals seeking to augment their existing careers with green, or climate-related skills.

Explore India's foreign affairs strategy through an insightful discussion featuring Shivshankar Menon, former National Security Advisor to the Prime Minister of India, and Tanvi Madan, Director of the India Project and Senior Fellow at Brookings. Moderated by Anja Manuel, Director of the Aspen Strategy Group, this 27-minute talk delves into the complexities and nuances of India's approach to international relations, offering valuable perspectives on the country's diplomatic priorities and global positioning.

Watch two insightful presentations from Stanford's medical faculty exploring the intersection of creativity, artificial intelligence, and academic medicine. Learn how Dr. David Hindin, Associate Chair of Innovation in Surgery, discusses transforming academic work through design principles and storytelling techniques, while Dr. Robert Chang, Associate Professor of Ophthalmology, delves into the creative applications of AI tools in medical academia. Gain valuable perspectives on innovating academic medical communication and leveraging emerging technologies to enhance both teaching and research presentation methods during this 58-minute Grand Rounds session from Stanford's Otolaryngology department.

Number of Credits :-4 Myself, Dr Ajay Semalty, from HNB Garhwal University (A Central university) Srinagar Garhwal (Uttarakhand) welcome you on behalf of our entire teamin the new cycle of our course.After the five successful run of the course, we are proud to present India's most popular SWAYAM MOOC which gotmaximum number of exam registration (among all the SWAYAM MOOCs) and has been listed in top 30 MOOCs worldwide (http://tiny.cc/pib27april2020;Course in News:http://tiny.cc/AWnews). Recently, the course has been listed in Class Central’s Best Online Courses of All Time (2021 Edn.). So far, more than 46000 learners across more than 150 countries have taken the course.In academic and research, who does not want the publications? In spite of being the vital requirement in academic & research career there is no comprehensive set up of learning academic writing in the knowledge domain. This course aims to fill this gap by providing the fundamental knowledge required for effective and result oriented academic writing. It is a foundation course and the application of this knowledge completely depends on an individual learner and his or her area of research.Objectives of CourseUpon completing the course, one would be able1. To differentiate between various kind of academic writings.2. To identify and avoid the plagiarism.3. To practice the basic skills of performing quality literature review.4. To practice the basic skills of research paper, review paper and thesis writing.5. To target the research work to suitable journal and communicate for publication6. To practice the Time and team management.7. To practice digital writing or develop Open Educational Resources (OER).8. To write research proposals, conference abstract and book chapters/ book proposals.Target GroupAny student or learner who wants to learn the academic writing. The course shall be helpful for PG students, research scholars, young scientists and faculty members (of any discipline or subject) for their career growth.Learn more about the course gcbTagYoutubeEnqueueVideo("yQ0LTLJDrQM", "zzVydxfWl7on");Testimonials from learners"....I was looking for such type of course for many years and finally, you fulfilled my wish to know more about research, guidelines about research, plagiarism, open educational resources, paper writing, thesis writing and many such significant topics for a researcher to know and understand about the various aspects of research." - Dr Anil PatilIt is a great experience. Just like it is a face to face classroom learning. The course providers actually from science faculty even though any one can access in such a way they provided all the information. Their tagged notes to the video is very useful for those who may not interact in web classes. -G. Satyanarayana,Asst. Professor, English."The course is interesting, creating curiosity, enthusiasm, educative, stimulating for a professional career. It is useful for practicing teaching faculty, researcher, and professionals. The presentation and transcript are useful and interesting. The presentation is clear, complete and effective. The quiz questions are interesting and challenging." -V.Chandra Sekhara RaoTeam AWDr Ajay Semalty(Course Coordinator & Subject Matter Expert)Dr Mona Semalty(Co-Course Coordinator & Subject Matter Expert)Prof Rajat Agrawal(Subject Matter Expert)Dr Lokesh Adhikari(Instructional Designer)Pandavaas Creations Pvt. Ltd.ProductionandTeam EMRC Roorkee

The course focuses on enhancing academic writing understanding and skills, providing essential foundational tools for success. For school leavers, it bridges the gap between prior education and tertiary requirements, while for professionals returning to higher education, it ensures effective communication of ideas in an academic setting. The course incorporates material to address AI technology's increasing influence on academic writing. This AI module stands as an independent section, allowing review and updates without disrupting the coherence of the entire course.

Explore a comprehensive series of lectures and tutorials on economy and current affairs tailored for UPSC and IAS exam preparation. Delve into crucial topics like shell companies, money laundering, insolvency and bankruptcy code, agricultural futures, finance commissions, external sector economics, budget analysis, and economic surveys. Learn about important economic concepts, policies, and current events through detailed explanations, MCQs, and weekly current affairs updates. Cover a wide range of subjects including inflation, banking, trade agreements, monetary policy, fiscal policy, and more. Gain insights into recent economic developments, government schemes, and their implications for competitive exams. Enhance your understanding of complex economic issues and prepare effectively for UPSC and IAS examinations with this extensive collection of educational content.

Explore the impact of the Veterans Affairs National Abdominal Aortic Screening Program in this 51-minute seminar presented by Dr. Manuel Garcia-Toca, Clinical Professor of Surgery and Chief of the Division of Vascular Surgery at Santa Clara Valley Medical Center. Gain insights into the effectiveness and outcomes of this crucial screening initiative designed to detect abdominal aortic aneurysms in veterans. Learn about the program's implementation, its significance in preventive healthcare, and how it has influenced patient care and outcomes within the VA healthcare system. Understand the latest developments in abdominal aortic screening techniques and their potential applications beyond the veteran population.

DRA, Orange book, USFDA, eCTD, CTD, INDA, NDA, ANDA, DMF, ICH, Software Demo, RA Jobs, Quiz, Pharma Skills, Updated 2025 What you'll learn: Basic concepts Pharma Regulatory AffairsAdvanced Regulatory AffairsHow Regulatory Authorities Regulates Drug productCareer in Regulatory AffairsJob opportunitieseCTD & CTD StructureeCTD ModulesDossier Preparation & SubmissionDrug master fileSubmission of Drug Master FileGeneral Demonstration of eCTD SoftwareGeneral demonstration of eValidatorRegistration ProcessICH GuidelinesUSFDA regulations: INDAINDA conceptNew drug developmentFDA meetingsIND Review processMarket ApprovalsOnline ESG (Electronic Submission Gateway) tool Are you looking for Regulatory affairs Jobs in 2024 and want to make a career in Pharmaceutical Regulatory affairs? Answer:If you are looking for Pharma Regulatory affairs course to start career as Regulatory Professional without paying huge amount or money then you are on right platform with best pilot.This updated course is for starting career and growing in existing profession as in Regulatory affairs with certificate of completion. Complete the course as per your free time as life time access is available. Course Details:The Pharmaceutical industry discovers, develops, produces, and markets drugs or pharmaceutical drugs for use as medications to be administered to patients, with the aim to cure them, vaccinate them, or alleviate the symptoms. Pharmaceutical companies may deal in generic or brand medications and medical devicesRegulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. ... Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug. So, this online course helps Pharmacy Students and Professionals to build their knowledge and skills towards career in Regulatory Affairs.Regulatory course prepares students to be skilled in the field of global regulatory affairs, and enables existing regulatory affairs professionals to refine and update their knowledge of global regulatory affairs statutes and practices.Prepare to play a pivotal role in managing the regulatory activities necessary to bring drugs and medical products to market. Learnings from this course:Global regulatory frameworks (FDA, EMA, CDSCO, MHRA, TGA, and more)Drug approval pathways (IND, NDA, ANDA, BLA)CTD & eCTD dossier preparationClinical trial regulations & GCP Why to choose this course:Designed by industry experts with hands-on regulatory experienceUp-to-date content based on current global standardsBoost your job-readiness in pharma, biotech, and CRO sectorsLearn how to work across global markets with confidenceCertificate of Completion to enhance your professional profileContents of this course :-A. Basics of Regulatory affairs1. Basic Regulatory Introduction2. Career and opportunities in RA3. Objectives in RA Profession4. Websites and Usage 5. Intoduction to ICH Guidelines6. Basic general information about DMF (Drug Master File)7. DMF preparation and submissionB. CTD & eCTD8. Module 19. Module 210. Module 311. Module 412. Module 513. eCTD software demo and eValidation C. Types of Application14. IND (Investigational New Drug Application)15. NDA (New Drug Application)16. ANDA (Abbreviated New Drug Application)D. Registration and Submission17. Introduction to ESG Gateway18. Overview of Registration Process19. FDA ESG web interface and electronic submission# Complimentary Quizes (Question & Answer) Eligibility RequirementsEducation and experience:A minimum of a baccalaureate or equivalent Lifescience subjects ORBachelors of Pharmacy, Masters of Pharmacy, Ph.D In Pharmacy, Industrial ProfessionalA master’s degree of regulatory or regulatory-related experience; ORA doctorate degree (e.g., medical, dental degree, PharmD, PhD, ScD, JD) and at least one year regulatory or regulatory-related experienceNo Prerequisite required only need Curiosity over new learnings Regulatory Certification Benefits for ProfessionalsAnyone who works in the life science arena should consider the RAC program as an educational supplement to one’s current work environment. As identified in the RAC Certification, earning a RAC is useful in a variety of professional settings, within regulatory agencies, government and inter-governmental bodies, industry, consultancies, professional organizations, healthcare facilities, research institutions and educational institutions around the world.Confidence is a true benefit from adding the RAC to your signature line, as a regulatory professional.Course is designed to cover all aspects of healthcare product regulations, compliance and standards, giving a global perspective on regulatory affairs. There are practice exams available online to help prepare.Certification by a Regulatory Professional platform not only gives you confidence in forming your regulatory advisements but also inspires confidence in those working with you or for whom you work. There is recognition that, by pursuing a regulatory certification, you have studied the regulations in your particular regulatory product area and are well versed in these regulations as well as in other product categories.The ability to pass an exam written by your peers in your specific area of regulatory responsibility affirms that regulatory professionals have a clear understanding of the core components within their specialty area. In this Advanced RA course the Detailed Practical and Theoretical aspects of Regulatory affairs can be learned in this course.Like :-Basics of Regulatory affairsICH, DMF, ASMF, CTD, eCTD, CTD structure, 1-5 Modules of CTD.Basic Demonstration of eCTD software & eValidator (Lorenz Docubridge) 21CFR complied. Drug Product Development, Documents Required for filling.Preperation & Submission of CTD, eCTD, DMF, Filling of Applications (IND, NDA, ANDA, BLA).Other miscellaneous Aspects in RA.Stringent GMPs are being followed for blood and its derivative as well as controlled manufacturing for Traditional Herbal Medicines, Cosmetics, Food and Dietary products which was otherwise differently a century before. Each regulatory system had faced certain circumstances which led to current well-defined controlled regulatory framework. This course contains Commonly Asked Questions and Answers for interview that will help you while preparing for DRA interviews.Last but not the least, this course also contains a bonus software demo entitled "General Demonstration and eValidation " which will help you to shape your career in which the points that must be taken into consideration while Preparing and submission of Dossier are covered.In this course, more than 42 informative videos are included and are designed in an easily digestible format and going to take you through step by step approach to understand Drug Regulatory Affairs and relevant activities. This course will help you to develop the ability to conduct regulatory intelligence and develop a regulatory strategic plan.I believe "Quality improvement is a continuous and lifetime process". Upon completion of this course, you will be a whole different professional with improved DRA skills and knowledge which will help you to garner more respect from your team members, managers, clients, or anyone with whom you are communicating/interacting.

Explore the impact of anti-Asian violence and discrimination in this insightful talk by Stanford psychiatrist Rona Hu, MD. Delve into the alarming rise of hate incidents against Asian Americans and Pacific Islanders since March 2020, with a focus on the 150 percent increase in major US cities. Examine the mental health consequences of both COVID-19 and the surge in hate crimes on Asian American communities. Learn about strategies to combat racism and violence against Asian Americans, as well as approaches for healing. Gain valuable insights from Dr. Hu's expertise as the Associate Dean of Academic Affairs at Stanford University School of Medicine, Clinical Professor of Psychiatry, and founder of initiatives like SMHART clinic and Stanford CHIPAO. Discover additional resources for health information and mindfulness practices offered by Stanford Health Library to support your well-being and understanding of this critical issue.

A practical primer discussing the EU Medical Device Regulation (EU MDR 2017/745) in real-world situations. What you'll learn: Learn about the new EU Medical Device Regulations and how it will impact different medical devices.Understand how to obtain CE Marking under the Medical Device Regulations.Complete real-world examples and exercises to apply the Medical Device Regulations to mock medical devices. The EUMedical Device Regulations (MDR 2017/745) represents the biggest change to medical device legislation in Europe for over 20 years. The MDRaffects all medical device manufacturers (and others!) wanting to sell devices in the EU. This course focuses on the practical application of the MDR, using real-world examples and exercises to help you understand not only what the Regulations mean, but what we need to do to comply with them.First written in 2020, this course quickly became the best-selling regulatory affairs course on Udemy with over 1,700 students enrolled. Now updated in 2025 with all the latest information, templates and resources to help you navigate EU medical device regulations. This is the perfect entry point for anyone looking to understand how medical devices are regulated in the EU, with several opportunites available for guided learning and deep dives into more detailed topics of interest, specific to your device or needs. We also discuss how to leverage EUmarket approvals in other global markets of interest.Written and developed by a group of Regulatory Affairs professionals currently working in industry, this course focuses on the most common issues and questions we receive from medical device manufacturers looking to enter the market under MDR.

Master Drug Approvals, FDA/EMA Compliance & Global Submissions | 2025 Career Guide for Pharma Professionals What you'll learn: Establish a solid foundation in pharmaceutical industry fundamentals and the critical role of regulatory affairs.Compare major global regulatory bodies and master FDA, EMA, PMDA, WHO, and moreNavigate drug development stages and submission processes from IND to NDA, ANDA, and beyondImplement GLP, GCP, and GMP standards while optimizing quality systems, audits, and compliance strategiesDesign ethical clinical trials, ensure patient rights, and handle safety reporting with integrityDevelop winning regulatory strategies, gather intelligence, and interact effectively with global health authoritiesOversee post-market safety monitoring, manage risk, and ensure product integrity across global marketsExplore advanced topics in biologics, medical devices, veterinary drugs, and other specialized regulatory domainsExamine global cooperation, address regional challenges, and streamline worldwide pharmaceutical complianceAdopt eCTD, leverage AI and blockchain, and embrace digital health innovations for modern regulatory processesUphold ethical standards, combat corruption, and safeguard intellectual property in regulatory practiceAnticipate emerging trends, navigate global crises, and shape the future of regulatory science and policy Your Fast Track to Global Drug LaunchesTurn regulatory hurdles into career-defining wins with the most complete online Regulatory Affairs course—20+ hours of focused, up-to-date training created for scientists, project managers, and health-tech entrepreneurs who need approvals first time, every time.Why this program?All-in-one mastery (20+ hours). Forget scattered webinars and outdated PDFs. You get a single, end-to-end roadmap covering every stage of drug development, dossier assembly, review cycles, and post-approval vigilance.Walkthroughs that actually walk. We’re the only course that hands you real launch blueprints—screen-recorded, step-by-step demos showing exactly how a submission moves from your desktop to agency approval.Learn exactly when—and how—you need it. Binge-watch a module on bioequivalence during your commute or revisit GMP theory before an audit. Lifetime, on-demand access means the knowledge is ready whenever you are.5+ hours of immersive case studies. Prefer doing over reading? Dive straight into four full product launches—FDA (USA), EMA (EU), NMPA (China), and CDSCO (India). See every form, timeline, and common pitfall before you face them in real life.What you’ll gainFluency with global health authorities—speak their language, anticipate objections, and resolve queries fast.Submission strategies that shave months off approval cycles, saving your company millions in lost market time.A portfolio of real-world launch playbooks you can deploy on Day 1 of your next project.Enroll now and become the regulatory strategist every pharma team is searching for.

"International Communication and East Asian Affairs: International News Practice" is an online course offered by the Graduate Institute of Journalism, National Taiwan University, in collaboration with Radio Taiwan International. This course delves into the practice of international news reporting within the context of East Asian affairs. Topics covered include non-fiction reporting techniques, the evolution and historical significance of radio in shaping communication landscapes, the detection of stance using large language model technologies, and strategies for identifying and debunking misinformation generated by AI. Throughout the course, learners will engage in video lectures and interactive discussions to deepen their understanding of international news practices. Whether pursuing advanced studies in international communication or preparing for enrollment in the Graduate Institute of Journalism at National Taiwan University, this course offers valuable insights and practical skills essential for effective global news coverage.

“International Communication and East Asian Affairs (1): Trends in International Communication” is the online course provided by the Graduate Institute of Journalism, National Taiwan University and Radio Taiwan International. This course provides learners an introduction to the international communication system with a focus on Taiwan and the Asian region. It includes the topics of introduction to international communication, international news flow, media technology and media transformation, cultural identity and the construction of national brand, and some related issues. Learners will attain a brief understanding of Taiwan’s international communication system and its transition in recent years. Each week we will focus on different aspects of international communication. Video lectures and discussions are included to enable you to learn about the key issues. Whether taking this as an independent course, for advanced international communication practice, or as preparation for the Graduate Institute of Journalism degree at National Taiwan University, you will find this course interesting and helpful.

Pharma course (NDA, ANDA, CTD, DMF, USFDA, Regulatory strategy, GMP, Clinical Research, Orange Book, Pharmaceuticals) What you'll learn: Basic understanding and terminologies related to Dug Regulatory Affairs (DRA).Why Regulatory Affairs (RA) professional is required in Pharma Industry and essential qualities of RA professionals.Understand the role of a Regulatory Affairs Professional in Pharmaceutical industry, Types of companies hiring RA professionals, and DRA objectives.Navigation through historical background of US Drug Law and Regulations, and The USFDA regulations for Research and Development (R&D) of Pharmaceuticals.Major Agencies for drug regulations In USA and other Countries (Along with downloadable website hyperlinked PDFs).Drug approval process in USA, New drug development-Preclinical Steps, IND, NDA, ANDA, Hatch-Waxman Act, etc.Orange book, Therapeutic Equivalence Evaluations Codes.Drug Master File- Related Terms, benefits, Annual update, Database status, Requirements, Process, Types, etc.)Common Technical Document (CTD), Modules, ACTD Vs ICH-CTD.Electronic Common Technical Document (eCTD), eCTD technical components, eCTD submissions, Paper CTD Vs eCTD , Various eCTD softwares.Good Manufacturing Practices (GMP) and Current Good Manufacturing Practices (cGMP).Clinical ResearchBiologics License Application (BLA) and Purple Book.Discover how to navigate important websites including ICH Guidelines to find more relevant information.Professional reputation building and career success enhancement through proper understanding of Drug Regulatory Affairs and related concepts. If you find the Drug Regulatory Affairs field challenging, well, in that case, this is the best course for you.The pharmaceutical industry is one of the extremely regulated industries, with several government regulations to protect public health. Therefore, the important target of the pharmaceutical industry is to develop a Drug product passing the regulatory requirements. On the other hand, regulation of drug development, manufacturing, marketing, and sales involves paradoxical objectives. It must ensure that safe and effective pharmaceutical formulations reach the public quickly while concurrently protecting against ineffective/unsafe/harmful therapies. Drug Regulatory authorities ensure the safety, efficacy, and quality of all pharmaceuticals that are in circulation in their country. The major challenge for the regulatory expert is to make sure that the pharmaceuticals are developed as per regulatory requirements of that country which involves the assessment of critical factors during the Drug product development. The United States Food and Drug Administration (USFDA) is one of the most regulated agencies wherein the Drug submission process is very strenuous and complicated. Understanding the crucial points in the Drug registration procedure will have a considerable impact on the accomplishment of its submission strategy. This course focuses on the following points that could make a Drug registration procedure smooth without any significant delays/failures,• Basic Understanding and Terminologies related to DRA,• Need and essential qualities of Regulatory Affairs Professional,• DRA objectives,• The USFDA regulatory requirements and Drug Approval Procedure,• History of US Drug Law and Regulations,• Investigational New Drug Application (INDA),• New Drug Application (NDA),• Abbreviated New Drug Application (ANDA),• Supplemental New Drug Application (SNDA),• Orange Book,• Drug Master File (DMF),• Common Technical Document (CTD),• Electronic Common Technical Document (eCTD),• Regulatory Strategy,• Good Manufacturing Practices (GMP) and Current Good Manufacturing Practices (cGMP),• Clinical Research,• Biologics License Application (BLA) and Purple Book,• Important Literature Search Websites for DRA Professional,• Many more...There will be several downloadable documents so that you can follow along with them whenever you need them.This course contains Commonly Asked Questions that will help you while preparing for DRA interviews.Last but not the least, this course also contains a bonus course entitled "Meeting etiquettes" which will help you to shape your career in which the points that must be taken into consideration while attending/conducting meetings are covered.In this course, more than 30 informative videos are included and are designed in an easily digestible format and going to take you through step by step approach to understand Drug Regulatory Affairs and relevant activities. This course will help you to develop the ability to conduct regulatory intelligence and develop a regulatory strategic plan.I believe "Quality improvement is a continuous and lifetime process". Upon completion of this course, you will be a whole different professional with improved DRA skills and knowledge which will help you to garner more respect from your team members, managers, clients, or anyone with whom you are communicating/interacting.

"International Communication and East Asian Affairs: Current Political and Economic Conditions" is an online course provided by the Graduate Institute of Journalism, National Taiwan University, and Radio Taiwan International. This course delves into East Asian affairs, particularly focusing on China and Taiwan. Topics covered include China's Third Revolution and its implications for the Sino-American strategic competition, the political economy of China, state-society relations within China, and an exploration of recent youth politics in Taiwan. Each week, the course provides comprehensive video lectures and interactive discussions to facilitate deeper understanding and engagement with the subject matter. Whether taken as part of advanced international communication studies or as preparation for enrollment in the Graduate Institute of Journalism at National Taiwan University, this course delivers intellectual stimulation and is instrumental in understanding contemporary global dynamics and East Asian affairs.

This course will introduce you to the basic elements of academic information seeking - we will explore the search process from defining a strategy to evaluating and documenting your search results. Attending the course will make you a proficient information seeker. You will learn how to carry out comprehensive literature searches based on your own research assignment. You will be guided through the various information seeking steps from selecting relevant search strategies and techniques to evaluating your search results, documenting your search process and citing your sources. Attending the course will enable you to: • Identify your information need • Evaluate databases and other information resources • Set up search strategies and use various search techniques • Formulate search strings based on your own research assignment • Identify relevant material types • Undertake critical evaluation of your sources • Search more efficiently on the internet • Avoid plagiarism • Cite correctly • Work with reference management • Document your search process The course is intended for undergraduate students but the lessons will be useful to anyone who is interested in becoming better at finding scientific information. There are no formal requirements for the course. The series consists of 21 lectures that are organized into three modules. The lectures include small assignments and quizzes (to check comprehension). The lectures will each touch upon a topic that is essential to the information seeking process. To get the most out of the lecture series, we recommend that you access the lectures while you are working on an academic paper. We also recommend that you watch the lectures in the order in which we have structured them. We recommend that you create and fill out a log book while attending the lectures. We have created a log book template that you can use during the course. The lecture series has been developed in collaboration between information specialists at University of Copenhagen and Technical University of Denmark

The skills taught in this Specialization will empower you to succeed in any college-level course or professional field. You’ll learn to conduct rigorous academic research and to express your ideas clearly in an academic format. In the final Capstone Project, all the knowledge that you’ve gained over the span of these courses will culminate into an academic research paper on an issue of your choice.

Explore a powerful TEDx talk that challenges perceptions of academic language and personal impact. Join Bryan Tapia, a first-generation Hispanic student at John Jay College of Criminal Justice, as he shares his journey from growing up in a low-income household in Washington Heights to pursuing a career as a lawyer in the financial district. Discover how Tapia's experiences shaped his passion for education and his goal to become a role model for future generations of Hispanic students. Learn about his vision to create an organization that helps marginalized groups fund their education and improve their financial literacy. Be inspired by Tapia's message that one's impact on the world, both large and small, should define a person rather than their way of speaking.

Do you want to read and write better in English? Welcome to our course. The course consists of 6 units with different topics: art, man and nature, social issues, engineering and technology, psychology, economics and management. From this course, you will have a good knowledge of general academic English learning skills. We invite you to learn with our teachers and friends from different countries in the videos. Are you ready? Let’s go!