Pharmaceutical drug business intelligence - DrugPatentWatch

Course Feature

Cost

Paid
Provider

Udemy
Certificate

Paid Certification
Language

English
Start Date

2021-10-05
Learners

No Information
Duration

No Information
Instructor

Yali Friedman, Ph.D.

Add to Favorites

4.1

301 Ratings

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.

Show All

Go to class

Course Overview

❗The content presented here is sourced directly from Udemy platform. For comprehensive course details, including enrollment information, simply click on the 'Go to class' link on our website.

Updated in [July 27th, 2023]

This course provides learners with an understanding of the most influential events in the pharmaceutical drug business. It covers commercial, legal, and regulatory factors, and provides actionable intelligence to help learners anticipate market-shaping forces and stay ahead of the competition. Through case studies and real-world examples, learners can gain an 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 experience providing guidance to drug development companies and other healthcare stakeholders, this course includes a free companion textbook.

Course Syllabus

Introduction

Innovative and Follower Drugs

Patents and Other Forms of Intellectual Property

Regulatory Exclusivity

Analyzing patents and litigation

Market Size and Quality

Branded Drug Launch and Lifecycle Management Strategies

Generic Portfolio Management

Conclusion

Extra - Conference Presentations

Show All

Recommended Courses

Introduction to Drug Discovery and Drug Development

4.1

Udemy 212 learners

Learn More

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!

Good Laboratory Practices

4.5

Udemy 176 learners

Learn More

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.

Part 11 Compliance for Computerised Systems

3.0

Udemy 188 learners

Learn More

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.

Data Integrity requirements for Pharmaceuticals

3.6

Udemy 164 learners

Learn More

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.