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⇱ Drug Development | Coursera


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Gain insight into a topic and learn the fundamentals.
4.7

2,429 reviews

Beginner level
No prior experience required
Flexible schedule
1 week at 10 hours a week
Learn at your own pace
95%
Most learners liked this course

Gain insight into a topic and learn the fundamentals.
4.7

2,429 reviews

Beginner level
No prior experience required
Flexible schedule
1 week at 10 hours a week
Learn at your own pace
95%
Most learners liked this course

Details to know

Shareable certificate

Add to your LinkedIn profile

Assessments

6 assignments

Taught in English

Build your subject-matter expertise

This course is part of the Drug Development Product Management Specialization
When you enroll in this course, you'll also be enrolled in this Specialization.
  • Learn new concepts from industry experts
  • Gain a foundational understanding of a subject or tool
  • Develop job-relevant skills with hands-on projects
  • Earn a shareable career certificate

There are 7 modules in this course

The University of California San Diego, Skaggs School of Pharmacy and Pharmaceutical Sciences Drug Development course brings you lectures from both faculty and industry experts. With this course, recorded on campus at UCSD, we seek to share our access to top people in the field who bring an unprecedented range of expertise on drug development.

In this course you will learn the different stages of clinical development as well as the regulatory including but not limited to, an Investigational New Drug Application (IND), New Drug Application (NDA), and product labeling. Additionally you will learn how to Incorporate study design methods for consideration in the design of clinical protocols to assess safety, tolerability, and efficacy in multiple therapeutic areas. In this course you will learn the different phases of clinical development: * Phase 1 or early stage clinical trial are conducted primar­ily to determine how the new drug works in humans, its safety profile and to predict its dosage range. It typically involves between 30 and 100 healthy volunteers. * Phase 2 or Proof of Concept POC studies test for efficacy as well as safety and side effects in a group of between 30 to 200 hundred patients with the disease for which the new drug is being developed. * Phase 3 or late stage clinical development involve much larger group of patients, between a few hundred to thousands, depending on the indication, which will help determine if the new drug can be considered both safe and effective. It will involve control groups using placebo and/or current treatment as a comparison. * Product registration and approval process after a drug is considered safe and effective from Phase 3 trials, it must be authorized in each individual country before it can be marketed. All data gen­erated about the small molecule or biologic is collected and submitted to the regulatory authorities in the US at the FDA, Food and Drug Administration FDA, in Europe the EMA or European Medicines Agency, Japan Ministry of Health and other countries which may require their own national approvals. This course is intended as part 2 of a series: Drug Discovery (https://www.coursera.org/learn/drug-discovery), Drug Development and Drug Commercialization (https://www.coursera.org/learn/drug-commercialization). We would highly recommend that you take the courses in order since it will give you a better understanding on how a drug is discovered in the lab before being tested in clinical trials and then launched in the market place.

What's included

1 video

1 videoTotal 3 minutes
  • Welcome!3 minutes

This week we hear from Dr. Susan Trieu, who in her 12+ years in the industry has worked in regulatory affairs. Since then, Dr. Trieu has gone on to work in Industry at MedImpact as their Drug Information Pharmacist.

What's included

5 videos2 readings1 assignment3 discussion prompts

5 videosTotal 46 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application I10 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application II11 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application III10 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application IV9 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application V6 minutes
2 readingsTotal 10 minutes
  • Lecture Slides0 minutes
  • A new Master Degree in Science in Drug Development & Product Management at UCSD10 minutes
1 assignmentTotal 30 minutes
  • Regulatory Considerations When Filing an Investigational New Drug Application Quiz30 minutes
3 discussion promptsTotal 30 minutes
  • How do high user fees impact drug development?10 minutes
  • The FDA's impact on drug development?10 minutes
  • Share interesting findings from ClinicalTrials.gov10 minutes

This module is presented by Dr. Joseph Ma, Associate Professor in the UCSD Skaggs School of Pharmacy and Pharmaceutical Sciences.

What's included

5 videos1 reading1 assignment1 discussion prompt

5 videosTotal 43 minutes
  • Clinical Study & Start-up Activities I11 minutes
  • Clinical Study & Start-up Activities II11 minutes
  • Clinical Study & Start-up Activities III7 minutes
  • Clinical Study & Start-up Activities IV6 minutes
  • Clinical Study & Start-up Activities V9 minutes
1 reading
  • Lecture Slides0 minutes
1 assignmentTotal 30 minutes
  • Clinical Study & Start-up Activities Quiz30 minutes
1 discussion promptTotal 10 minutes
  • What do you think are the most important ethical concerns?10 minutes

This module we will hear from Dr. Yazdi Pithavala, Senior Director, Clinical Pharmacology at Pfizer.

What's included

5 videos1 reading1 assignment1 discussion prompt

5 videosTotal 46 minutes
  • Clinical Trials: Phase 1 Part I10 minutes
  • Clinical Trials: Phase 1 Part II10 minutes
  • Clinical Trials: Phase 1 Part III12 minutes
  • Clinical Trials: Phase 1 Part IV9 minutes
  • Clinical Trials: Phase 1 Part V5 minutes
1 reading
  • Lecture Slides0 minutes
1 assignmentTotal 30 minutes
  • Clinical Trials: Phase 1 Quiz30 minutes
1 discussion promptTotal 10 minutes
  • Other major safety Phase I situations?10 minutes

Next we hear from Kourosh Parivar, M. Pharm, Vice President & Head, Clinical Pharmacology at Pfizer

What's included

5 videos1 reading1 assignment1 discussion prompt

5 videosTotal 47 minutes
  • Clinical Trials: Phase 2 Part I10 minutes
  • Clinical Trials: Phase 2 Part II11 minutes
  • Clinical Trials: Phase 2 Part III11 minutes
  • Clinical Trials: Phase 2 Part IV10 minutes
  • Clinical Trials: Phase 2 Part IV5 minutes
1 reading
  • Lecture Slides0 minutes
1 assignmentTotal 30 minutes
  • Clinical Trials: Phase 2 Quiz30 minutes
1 discussion promptTotal 10 minutes
  • How do you see changing medical technology impacting Phase II studies?10 minutes

What's included

5 videos1 reading1 assignment3 discussion prompts

5 videosTotal 44 minutes
  • Industry Considerations with Phase III Clinical Trials I11 minutes
  • Industry Considerations with Phase III Clinical Trials II11 minutes
  • Industry Considerations with Phase III Clinical Trials III11 minutes
  • Industry Considerations with Phase III Clinical Trials IV7 minutes
  • Industry Considerations with Phase III Clinical Trials V5 minutes
1 reading
  • Lecture Slides0 minutes
1 assignmentTotal 30 minutes
  • Industry Considerations with Phase III Clinical Trials Quiz30 minutes
3 discussion promptsTotal 30 minutes
  • Share other globally influenced drug discoveries!10 minutes
  • Share a collaboration story...10 minutes
  • What other values do you see in running studies in a variety of countries?10 minutes

What's included

6 videos1 reading1 assignment2 discussion prompts

6 videosTotal 55 minutes
  • New Drug Application, Filing, Product Labeling I10 minutes
  • New Drug Application, Filing, Product Labeling II10 minutes
  • New Drug Application, Filing, Product Labeling III9 minutes
  • New Drug Application, Filing, Product Labeling IV9 minutes
  • New Drug Application, Filing, Product Labeling V10 minutes
  • New Drug Application, Filing, Product Labeling VI9 minutes
1 reading
  • Lecture Slides0 minutes
1 assignmentTotal 30 minutes
  • New Drug Application, Filing, Product Labeling Quiz30 minutes
2 discussion promptsTotal 20 minutes
  • Where do you get data on drugs?10 minutes
  • Drug Promotion: Good or Bad?10 minutes

Earn a career certificate

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Instructors

Instructor ratings
4.6 (561 ratings)
University of California San Diego
3 Courses223,283 learners
University of California San Diego
3 Courses223,283 learners

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Learner reviews

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Showing 3 of 2429

HD
·

Reviewed on Aug 2, 2020

Great introduction to the nuances of drug development, post research and into clinical and commercial aspects. I feel much more ready to enter the regulatory affairs arena after this.

MR
·

Reviewed on Jul 18, 2018

Information in the course is very practical. I come from basic biology background and now with this course I gained some real insights about how the clinical trails happen.

MS
·

Reviewed on Jul 13, 2020

I would have loved to have a specific case study to follow as an example of how a drug goes through the whole life cycle as the course felt a bit too high-level overview at times.

Frequently asked questions

To access the course materials, assignments and to earn a Certificate, you will need to purchase the Certificate experience when you enroll in a course. You can try a Free Trial instead, or apply for Financial Aid. The course may offer 'Full Course, No Certificate' instead. This option lets you see all course materials, submit required assessments, and get a final grade. This also means that you will not be able to purchase a Certificate experience.

When you enroll in the course, you get access to all of the courses in the Specialization, and you earn a certificate when you complete the work. Your electronic Certificate will be added to your Accomplishments page - from there, you can print your Certificate or add it to your LinkedIn profile.

Yes. In select learning programs, you can apply for financial aid or a scholarship if you can’t afford the enrollment fee. If fin aid or scholarship is available for your learning program selection, you’ll find a link to apply on the description page.

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