【2024年】十大製藥業課程熱門排行推薦與優惠精選!
本文章推薦「Your Guide to the Pharmaceutical Industry」、「Pharmaceutical Supply Management for Developing Countries」、「Basic Good Manufacturing Practices (GMP)」等相關LinkedIn線上課程,讓您滿足學習的慾望。
你是否想透過線上學習得到更多的技能,增加自己的技能樹?現在是學生的您,透過線上學習可以將更多專業知識用在課業學習上更加強所學。還是您是朝九晚五的上班族,尋找可以為工作上帶來更上一層樓的技能?或您是因為興趣或想培養其他興趣?
線上課程不受地理位置影響,不受時間早晚影響,老師來自世界各地,也不受學習程度影響的特色,讓您無時無刻想學都可以,想多看幾次增加熟悉度也可以。不同領域的老師將針對不同主題滿足您的學習目的,推薦的課程項目會陸續更新,絕對提供您最熱門人氣高的線上課程。
目錄
- Your Guide to the Pharmaceutical Industry
- Pharmaceutical Supply Management for Developing Countries
- Basic Good Manufacturing Practices (GMP)
- The Pharmaceutical R&D Process in Healthcare
- Global Pharma Regulatory Affairs course
- India Pharma Industry Course: Basics + Relevant Concepts
- Computerised System Validation (CSV)
- DrugPatentWatch: Generic & Branded Drug Launch and Lifecycle
- How to audit GMP systems
- Data Integrity requirements for Pharmaceuticals
製藥業課程總覽
課程資訊 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |
---|---|---|---|---|---|---|---|---|---|---|
評價 | 4.4 分 (1,655 個評分) | 4.5 分 (628 個評分) | 4.1 分 (444 個評分) | 4.3 分 (123 個評分) | 4.0 分 (87 個評分) | 4.3 分 (71 個評分) | 4.4 分 (31 個評分) | 4.5 分 (22 個評分) | 4.0 分 (9 個評分) | 4.1 分 (6 個評分) |
學生 | 4,247 人人 | 1,912 人人 | 908 人人 | 443 人人 | 331 人人 | 284 人人 | 172 人人 | 112 人人 | 40 人人 | 31 人人 |
課程描述 | Learn about the pharma industry quickly – current trends, medicines, healthcare, pharmacy markets & major developments | How to Select, Quantify, Procure, Store and Distribute Essential Medicines and Medical Supplies. Pharmacy Supply Chain | Learn the good practices that applies to the pharmaceutical industry | Learn about clinical trials, drug regulations, biotech products, generics, marketing and more. *COVID-19 Update 1/21* | Global Regulatory Affairs | Please read Course Description / Course Content and See the promo video for course details, expected learnings…. | This course will take to understand practical approach towards validation requirements | Pharmaceutical Industry and Biotechnology Patents and Branded & Generic Drug Market Entry Opportunities – FREE TEXTBOOK | Learn the basis and techniques to perform audits to GMP systems | Data Integrity in Analytical laboratories, in Microbiology laboratorie, Audit trial review, DI and Good doc. Practices |
製藥業課程列表
Your Guide to the Pharmaceutical Industry
課程老師 | Phil Yates |
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課程評價 | 4.4 分(1,655 個評分) |
學生人數 | 4,247 人 |
課程介紹
Are you interested in the pharma industry? Would you like to talk confidently about pharmaceuticals and healthcare?
The pharmaceutical industry is one of the most dynamic and exciting professions in the world. It can be hugely rewarding professiona
哪些人適合這堂課?
- An ideal course for newcomers or anyone interested in the industry looking to enhance their pharma knowledge
- Those looking to talk confidently and become better prepared for working with the pharmaceutical industry
- Students, Professionals, Businesses, Patients, Carers and anyone looking to build their expertise in the pharma industry
學習目標
- Learn essential facts about medicines and the structure of the pharmaceutical industry around the world
- Answer questions about the industry today and the major developments
- Explain where are the major markets and who are the major players
- Explain which drugs are the most successful
- Explain which disease areas are of greatest interest
- Discover how the industry has evolved and how the industry is adapting
Pharmaceutical Supply Management for Developing Countries
課程老師 | Ron Wehrens, M.Sc. Pharmacist MBA |
---|---|
課程評價 | 4.5 分(628 個評分) |
學生人數 | 1,912 人 |
課程介紹
Hi!
My name is Ron Wehrens and I’m a pharmacist from the Netherlands with 25 years of hands-on experience in pharmaceutical and medical supply management in developing countries.In case you are interested, you’ll find my CV available for download w
哪些人適合這堂課?
- Anyone interested in improving access to medicines and health products in low and middle income countries
學習目標
- Understand the pharmaceutical industry
- Pharmaceutical and healthcare needs in low and middle income countries
- Detailled insight in all steps of the supply cycle (e.g. Specification, Quantification, Procurement, Storage, Use)
- How to forecast/quantify medicines and health products
- Procurement
- Warehousing and distribution logistics
- Rational use of medicines
Basic Good Manufacturing Practices (GMP)
課程老師 | Ruben Alonso |
---|---|
課程評價 | 4.1 分(444 個評分) |
學生人數 | 908 人 |
課程介紹
The compliance with GMP (Good Manufacturing Practices) standards is the decisive aspect for the production of high quality products. They are mandatory for all Pharmaceutical laboratories, thus health authorities performs inspection and audits in ord
哪些人適合這堂課?
- Current Pharmaceutical industry employees
- People interested in entering the world of the pharmaceutical industry, regardless of the future position
學習目標
- You will learn the most important pharmaceutical regulation and its importance, obtaining a basic overview of the GMP requirements in pharmaceutical industry
- You will become familiar with the technical terms of the GMP field and their meaning.
- You will learn the fundamental parts of the pharmaceutical industry.
The Pharmaceutical R&D Process in Healthcare
課程老師 | James Mitroka |
---|---|
課程評價 | 4.3 分(123 個評分) |
學生人數 | 443 人 |
課程介紹
Are you curious about the drug R&D process? Are you considering a career in the pharmaceutical industry?
The discovery and development of medicines is one of the most interesting and impactful areas of human endeavor. And the pharmaceutical indus
哪些人適合這堂課?
- Anyone interested in knowing how drugs are discovered,developed, and marketed in the US.
學習目標
- Students will learn how modern drugs are discovered, developed and marketed by “Big Pharma” in accordance with FDA regulations.
課程老師 | Mahesh Pratapwar |
---|---|
課程評價 | 4.0 分(87 個評分) |
學生人數 | 331 人 |
課程介紹
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.
This course is for starting career in Regulatory affairs with certificate of compl
哪些人適合這堂課?
- Pharmaceutical industry employees
- Pharmacy Students & Pharma Professionals
- Chemistry students
- Science Graduates
- Diploma in pharmacy
- Pharma professionals
學習目標
- Basic concepts Pharma Regulatory Affairs
- Advanced Regulatory Affairs
- How Regulatory Authorities Regulates Drug product
- Career in Regulatory Affairs
- Job opportunities
- eCTD & CTD Structure
- Dossier Preparation & Submission
- Drug master file
- Submission of Drug Master File
- eCTD Modules
- General Demonstration of eCTD Software
- General demonstration of eValidator
India Pharma Industry Course: Basics + Relevant Concepts
課程老師 | Vikas Sonawale, PharmaC2C.com |
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課程評價 | 4.3 分(71 個評分) |
學生人數 | 284 人 |
課程介紹
Introducing a Pharma Course for Pharma/B.Sc students, graduates, industry professionals.
This course will help you with basic concepts related to the functioning of the Pharma Industry. The focus is on Indian market but we have given global touch so
哪些人適合這堂課?
- Anyone who is looking to get entry in Pharmaceutical Industry
- Existing Pharma Professionals who are looking to progress in their jobs
學習目標
- Indian Pharmaceutical Industry – Basics and other relevant concepts
- By the End of this course, you will have full understanding of Basic Pharma Concepts including types of drugs, company business models, relevant companies and their drugs and much more.
- This course covers relevant topics which will help you in passing your job interviews.
Computerised System Validation (CSV)
課程老師 | Hitendrakumar Shah |
---|---|
課程評價 | 4.4 分(31 個評分) |
學生人數 | 172 人 |
課程介紹
This course has been updated to include the update on 21 CFR Part 11 and also electronic version of CFR part 11. This fundamental course introduces participants to regulatory requirements for computerized systems in the pharmaceutical industry and ex
哪些人適合這堂課?
- Pharmacy students, consultants who are doing computerised system validation, This course is essential for software vendors, auditors, and quality staff involved in GxP applications. • Regulatory Affairs • QA/ QC • IT/IS • Software Managers • Project Managers • Software vendors and suppliers
學習目標
- Pharmacy,
- This course has been updated to include the update on 21 CFR Part 11 and also electronic version of CFR part 11. This two-day fundamental course introduces participants to regulatory requirements for computerized systems in the pharmaceutical industry and explores tried, tested, and internationally recognized methods of meeting those requirements. Regulatory guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements. The course will provide principles and an overview of the overall computer systems compliance.
DrugPatentWatch: Generic & Branded Drug Launch and Lifecycle
課程老師 | Yali Friedman, Ph.D. |
---|---|
課程評價 | 4.5 分(22 個評分) |
學生人數 | 112 人 |
課程介紹
Want insights into the biggest revenue-changing events?
By tracking patent expirations, patent litigation, generic and biosimilar development, you can anticipate these market-shaping forces and stay one step ahead.
Branded drug companies can experi
哪些人適合這堂課?
- Generic pharmaceutical company portfolio managers
- Branded drug lifecycle management, sourcing, procurement, and supply chain professionals
- Pharmaceutical drug analysts, investment analysts, and patent analysts
- Patent analysts
- Patent Landscape Profilers
- Biotech and Pharma Investors
- Supply chain, sourcing, purchasing managers, procurement, wholesalers, distributors, and warehouses
- Good Manufacturing Practice (GMP) facility owners and operators
- Pharmaceutical regulatory affairs professionals, lawyers, consultants, and founders
- Drug and medical device development managers
學習目標
- Finding and evaluating generic drug market entry opportunities
- Branded drug lifecycle management
- Find generic drug entry opportunities
- Track drugs in development and explore new indications for existing drugs
- Study failed patent challenges to develop a better strategy
- Collect competitive intelligence by examining contractual disputes
- Track litigation to anticipate early generic entry
- Find and evaluate business opportunities
- Assess levels of generic competition
- Use drug price ranges to evaluate price elasticity
- Determine optimal prices before launch
- Evaluate buyer power with data on reimbursement segmentation
- Align distribution methods with information on where and how drugs are purchased
- Evaluate branded and generic market opportunities globally
- Anticipate 505(b)(2) and biosimilar approvals
- Strengthen new formulation patents by studying prior claims and litigation
- Adapt your gmp facility to capture changes in demand with brand erosion and generic launches as drug patents expire
- Position regulatory affairs to capture emerging opportunities
- Understand the roles of patents, trade secrets, trademark, and other forms of intellectual property protection in protecting branded pharmaceutical and biotechnology drugs
- Proactively adapt sourcing, purchasing, and supply chain management to anticipate changes in supply and demand with generic drug entry
How to audit GMP systems
課程老師 | Ruben Alonso |
---|---|
課程評價 | 4.0 分(9 個評分) |
學生人數 | 40 人 |
課程介紹
Audits is one of the best tools to learn and understand the process and the quality system of any company. For this reason, internal audits to your company and audits to the pharmaceutical raw material suppliers are usually performed to ensure the qu
哪些人適合這堂課?
- Current pharmaceutical industry employees
- Employees from companies supplying products to pharmaceutical companies
- People interested in entering the world of the pharmaceutical industry which would like to have a deeper knowledge
學習目標
- General information on audits
- Which types of suppliers should be audited
- The audit process, how to plan and conduct audits efficiently
- Auditor behaviors and techniques, to face the various challenges
- How to audit API manufacturers
- Other interesting related topics
Data Integrity requirements for Pharmaceuticals
課程老師 | Hitendrakumar Shah |
---|---|
課程評價 | 4.1 分(6 個評分) |
學生人數 | 31 人 |
課程介紹
Data Integrity is one of the basic GMP principles since years multiple Data Integrity citations were reported by FDA und European inspectors during the last 3 years. Many US Warning Letters and EU Non-Compliance Reports deal with serious Data Integri
哪些人適合這堂課?
- Pharmacy students, Pharmaceutical professionals, consultants. This course is essential for software vendors, auditors, and quality staff involved in GxP applications. • Regulatory Affairs • QA/ QC • IT/IS • Software Managers • Quality heads • Software vendors and suppliers
學習目標
- This course has been updated to include brief understanding about data integrity requirements for pharmaceuticals with guideline requirements about data integrity, audit trail review, data integrity in production, data integrity in analytical laboratories and data integrity in microbiological laboratories
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參考其他產業線上課程
除了本文介紹的課程種類以外,想要瞭解產業領域還有哪些不同類型的課程值得一探究竟嗎?讓您可以從不同面向更紮實的學習,點擊參考以下其他熱門主題文章。絕對提供您最優惠人氣滿檔的課程,歡迎繼續延伸閱讀。