Free Online Pharmaceutical Industry Courses and Certifications 2024
The pharmaceutical industry develops, produces, and markets drugs or pharmaceuticals licensed for use as medications. Pharmaceutical companies may deal in generic or brand medications and medical devices. They are subject to a variety of laws and regulations regarding the patenting, testing and ensuring safety and efficacy and marketing of drugs.
Popular Courses
This Mybo Online Course on "Quality in Pharmaceutical Industry" offers a free three-week course to prior enrolled participants. On Day-2 Session (16th August 2020), the course focuses on "Six Sigma in the Pharmaceutical Industry". Prof. J. Vijaya Ratna, Retd. Professor of A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam, India, is the course instructor. Dr. Manthan D. Janodia, Professor and Head of the Dept. of Pharmacy Management, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, is the moderator. Join this free course to learn about Six Sigma in the Pharmaceutical Industry from experts in the field. Assessments are exclusively for prior enrolled candidates for certification. All communications will be done through closed virtual classrooms. Don't miss this opportunity to gain valuable knowledge and certification.
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This course provides a comprehensive overview of CTD, NeeS & eCTD, the unified global registration system for pharmaceutical and biological products. It explains the rationale for the CTD, NeeS & eCTD, and provides detailed guidance on its structure and format. Participants will learn how to prepare submissions to regulatory authorities in all countries or regions where the CTD/NeeS/eCTD formats are mandatory, recommended or accepted. The course also covers the differences between CTD, NeeS & eCTD, CTD/eCTD history, and criteria of dossier preparation. By the end of the course, participants should be able to confidently prepare and submit CTD/NeeS/eCTD dossiers.
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This course provides an introduction to two important unit operations used in the Pharmaceutical Industry: Size Reduction and Size Separation. It covers the effects of particle size on properties such as dissolution rate and powder flow characteristics, and explains the various size reduction and size separation methodologies and equipment used to obtain powders with desired particle sizes. It is ideal for those looking to gain a better understanding of the processes involved in the manufacturing of tablets, suspensions, ORS, and powder preparations.
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This online training course provides a comprehensive overview of Clean-in-Place (CIP) systems for the pharmaceutical industry. Participants will gain an understanding of engineering concepts, principles, and integration of CIP systems, Clean-out-of-Place (COP) systems, or immersion parts washers. The course will focus on the dynamics of CIP and COP technologies, with an emphasis on selecting the right cleaning chemistries for specific soil residues. Manual cleaning practices will also be discussed. This course is ideal for those looking to gain a better understanding of the fundamentals of cleaning in the pharmaceutical industry. Click now to learn more about this comprehensive online training course.
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This course, Pharmaceutical Drug Business Intelligence - DrugPatentWatch, provides learners with the knowledge and skills to stay ahead of the biggest revenue-changing events in the pharmaceutical drug business. It covers commercial, legal, and regulatory factors, and provides actionable intelligence to help learners anticipate market-shaping forces. Through case studies and real-world examples, learners can gain a better understanding of how to write stronger patents, defeat drug patents, find and evaluate generic market entry opportunities, and find proprietary out-of-court settlements and deal terms. With more than twenty years of providing guidance to drug development companies and other healthcare stakeholders, this course is the perfect opportunity to gain the skills and knowledge needed to stay ahead of the competition. Plus, a free companion textbook is included.
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This course provides learners with the knowledge and understanding of Good Distribution Practices (GDP-GMP). It covers the concepts that every employee from the pharmaceutical distribution industry must know and comply with, as well as the main departments and processes involved in a pharmaceutical distribution company. Upon completion, learners will be able to understand the importance of the GDPs and the requirements which will help them improve their daily work. They will also receive lifetime access to the course, personalized support, a certificate in “Good Distribution Practices” from Udemy, supportive documentation, questionnaires for practice, and a money-back guarantee in the first 30 days. This course is perfect for those looking to gain a better understanding of the pharmaceutical distribution industry.
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This course, Introduction to Drug Discovery and Drug Development, is perfect for those looking to expand their career knowledge into the pharmaceutical industry or aspiring pharmaceutical scientists and clinical project coordinators. It provides a deep understanding of the science behind drug discovery, development, clinical trials, alternative medicine, generic and innovator drugs, and regulatory affairs. Through real-life examples, you'll learn why theories work and how to apply them in your daily life. By the end of the course, you'll have a comprehensive understanding of the pharmaceutical industry. Don't miss out on this opportunity to become an expert in drug discovery and development!
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This course on Good Laboratory Practices will provide a comprehensive overview of data integrity in analytical and microbiology laboratories, as well as analytical method validations, stability studies, and human error investigations. Attendees will learn about FDA/EU Citations, ALCOA+ concept, audit trails in microbiology, and more. They will also gain an understanding of QBD approach, ICHQ14, ICHQ2(R1), and revalidation criteria. This course is essential for anyone looking to gain a better understanding of good laboratory practices.
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This course provides a comprehensive overview of Part 11 Compliance for Computerised Systems. It covers USFDA 21 CFR Part 11, EUGMP Annex 11, and Data Integrity requirements. Through discussion and learning videos, you will learn how to design systems and processes to ensure compliance, audit preparedness, and common errors to avoid. This course is essential for any pharmaceutical company looking to ensure their computerised systems are Part 11 compliant.
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This course provides a comprehensive understanding of the data integrity requirements for pharmaceuticals. It covers topics such as GMP principles, FDA and European inspector citations, US Warning Letters and EU Non-Compliance Reports, and international authority guidelines. Learners will gain an understanding of the data integrity requirements of a GMP regulated laboratory in pharmaceutical organisations and contract labs, and how laboratory personnel can ensure compliance and be able to defend their positions. The course also covers basics in data integrity and audit trail review, as well as the differences between good documentation Practices requirements and data integrity requirements. Specialised sessions focus on data integrity requirements for analytical laboratories and Microbiology laboratories. Join this course to gain a comprehensive understanding of data integrity requirements for pharmaceuticals.
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This course provides a comprehensive overview of Computer Aided Drug Design (CADD) from A to Z. It is suitable for anyone who wants to learn the basics and concepts of drug discovery and design drugs from scratch. Learners will gain an understanding of the relationships between physico-chemical properties of drugs and their biological activities, as well as the types of interactions between drugs and receptors. They will also be familiar with modern techniques such as computer-based methods of quantitative structural activity relationship QSAR and molecular graphics. This course covers all aspects of drug discovery, from sources of lead compound to drug latentiation (prodrug), and is perfect for anyone looking to gain a comprehensive understanding of CADD.
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This course provides an in-depth understanding of the pharmaceutical R&D process in healthcare. Through lectures, quizzes, activities, and opinion questions, learners will gain an understanding of how drugs are discovered, developed, and marketed, and the role of the FDA. It is designed for anyone considering a career in the pharmaceutical industry or anyone who would like to know more about the process. Learners will be able to evaluate job descriptions, select the appropriate career training courses and conferences, and confidently discuss opportunities with career counselors, recruiters, and people working in the pharmaceutical industry. This course is perfect for those looking to gain a comprehensive understanding of the pharmaceutical R&D process in healthcare.
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This course provides a comprehensive introduction to Computerised System Validation (CSV) for new learners. It covers topics such as categorisation of software and hardware as per GAMP 5, different validation strategies, developing URS, FRS, FAT, SAT, IQ, OQ and PQ, test strategies, validation master plan and validation master report concept, and common questions and answers. It is beneficial for regulatory, clinical, and IT professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors, as well as software vendors, auditors, and quality staff involved in GxP applications. This course explores tried, tested, and internationally recognized methods of meeting regulatory requirements for computerized systems in the pharmaceutical industry. Click now to learn more!
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This eCTD & CTD Preparation & Submission Course is the perfect way to gain a comprehensive understanding of the Electronic Common Technical Document (eCTD) specification. Learners will gain an understanding of the creation of an eCTD submission, and an overview of regional differences in dossiers. Upon completion of the course, learners will receive a certificate of completion and be equipped with the knowledge to pursue job opportunities in Regulatory Affairs, such as Regulatory Affairs Associates, Regulatory Affairs Assistance, Regulatory Affairs Head/Director, and Medical Information. This course is a valuable training and reference tool for those new to the use of the format, and can be of assistance to anyone involved with electronic submissions and navigating changing requirements. Don't miss out on this great opportunity to gain the skills and knowledge needed to pursue a career in Regulatory Affairs.
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This course provides a comprehensive overview of US Food & Drug Administration (FDA) regulations for biologics and pharmaceutical drugs. It is beneficial for scientists, physicians, entrepreneurs, public health professionals, industry analysts, consultants, and biomedical students interested in the biotechnology and pharmaceutical industry. Learners will gain an understanding of the importance of FDA regulations for public health, and how to navigate through the FDA regulations to market a biologic or pharmaceutical. They will also develop their ability to conduct regulatory intelligence and develop a regulatory strategic plan. This course is a great opportunity to gain knowledge of the drug development process and the key regulatory steps toward FDA approval.
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This course provides a comprehensive overview of the Quality Management System (QMS) in the pharmaceutical industry. Learners will gain an understanding of the three levels of quality, the role of management in the QMS, the objectives of the QMS, and how the elements of the QMS are integrated. They will also learn about the meaning and application of the QMS in the pharmaceutical industry, the quality standards and pharmacopeias behind it, the ISO, GMP, and GXP, and the importance of documentation. Finally, learners will gain an understanding of personnel training and process validation. Master pharmaceutical quality management system is the perfect course for those who want to gain an in-depth understanding of the QMS in the pharmaceutical industry.
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Frequently Asked Questions and Answers
Q1: What is in pharmaceutical industry?
The pharmaceutical industry refers to the sector involved in the discovery, development, and manufacture of drugs and medications (pharmaceuticals) by both public and private organizations.
Q2: What are the big 6 pharma companies?
The six largest drugmakers by 2021 revenue are Johnson & Johnson, Pfizer, Roche, AbbVie, Novartis, and Merck & Co.
Q3: What do you do in a pharmaceutical job?
There is a wide range of job roles available, including laboratory-based research and development, clinical trials, regulatory affairs, drug safety, manufacturing, engineering, quality assurance, quality control, validation, as well as marketing, sales, and distribution.
Q4: Is a job in the pharmaceutical industry good?
The pharmaceutical industry is recognized as a rapidly growing and dynamic field, providing numerous opportunities for individuals to establish a rewarding career. Irrespective of one's interests in science and research, technology and innovation, management, business, or any other domain, there is a high probability of finding a suitable role within this industry.
Q5: What is the largest pharma company in the US?
The five largest U.S. pharmaceutical companies by market cap, namely Eli Lilly, Johnson & Johnson, Merck, AbbVie, and Pfizer, have collectively reported earnings of $81.9 billion in 2022, as per an analysis conducted by Accountable.US. This marks an $8 billion rise from the previous year.
Q6: What Pharmaceutical Industry courses can I find on AZ Class?
On this page, we have collected free or certified 33 Pharmaceutical Industry online courses from various platforms. The list currently only displays up to 50 items. If you have other needs, please contact us.
Q7: Can I learn Pharmaceutical Industry for free?
Yes, If you don’t know Pharmaceutical Industry, we recommend that you try free online courses, some of which offer certification (please refer to the latest list on the webpage as the standard). Wish you a good online learning experience!
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