Drug Development
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Drug Development
This course is part of Drug Development Product Management Specialization
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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 video•Total 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 videos•Total 46 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application I•10 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application II•11 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application III•10 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application IV•9 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application V•6 minutes
2 readings•Total 10 minutes
- Lecture Slides•0 minutes
- A new Master Degree in Science in Drug Development & Product Management at UCSD•10 minutes
1 assignment•Total 30 minutes
- Regulatory Considerations When Filing an Investigational New Drug Application Quiz•30 minutes
3 discussion prompts•Total 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.gov•10 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 videos•Total 43 minutes
- Clinical Study & Start-up Activities I•11 minutes
- Clinical Study & Start-up Activities II•11 minutes
- Clinical Study & Start-up Activities III•7 minutes
- Clinical Study & Start-up Activities IV•6 minutes
- Clinical Study & Start-up Activities V•9 minutes
1 reading
- Lecture Slides•0 minutes
1 assignment•Total 30 minutes
- Clinical Study & Start-up Activities Quiz•30 minutes
1 discussion prompt•Total 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 videos•Total 46 minutes
- Clinical Trials: Phase 1 Part I•10 minutes
- Clinical Trials: Phase 1 Part II•10 minutes
- Clinical Trials: Phase 1 Part III•12 minutes
- Clinical Trials: Phase 1 Part IV•9 minutes
- Clinical Trials: Phase 1 Part V•5 minutes
1 reading
- Lecture Slides•0 minutes
1 assignment•Total 30 minutes
- Clinical Trials: Phase 1 Quiz•30 minutes
1 discussion prompt•Total 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 videos•Total 47 minutes
- Clinical Trials: Phase 2 Part I•10 minutes
- Clinical Trials: Phase 2 Part II•11 minutes
- Clinical Trials: Phase 2 Part III•11 minutes
- Clinical Trials: Phase 2 Part IV•10 minutes
- Clinical Trials: Phase 2 Part IV•5 minutes
1 reading
- Lecture Slides•0 minutes
1 assignment•Total 30 minutes
- Clinical Trials: Phase 2 Quiz•30 minutes
1 discussion prompt•Total 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 videos•Total 44 minutes
- Industry Considerations with Phase III Clinical Trials I•11 minutes
- Industry Considerations with Phase III Clinical Trials II•11 minutes
- Industry Considerations with Phase III Clinical Trials III•11 minutes
- Industry Considerations with Phase III Clinical Trials IV•7 minutes
- Industry Considerations with Phase III Clinical Trials V•5 minutes
1 reading
- Lecture Slides•0 minutes
1 assignment•Total 30 minutes
- Industry Considerations with Phase III Clinical Trials Quiz•30 minutes
3 discussion prompts•Total 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 videos•Total 55 minutes
- New Drug Application, Filing, Product Labeling I•10 minutes
- New Drug Application, Filing, Product Labeling II•10 minutes
- New Drug Application, Filing, Product Labeling III•9 minutes
- New Drug Application, Filing, Product Labeling IV•9 minutes
- New Drug Application, Filing, Product Labeling V•10 minutes
- New Drug Application, Filing, Product Labeling VI•9 minutes
1 reading
- Lecture Slides•0 minutes
1 assignment•Total 30 minutes
- New Drug Application, Filing, Product Labeling Quiz•30 minutes
2 discussion prompts•Total 20 minutes
- Where do you get data on drugs?•10 minutes
- Drug Promotion: Good or Bad?•10 minutes
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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.
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.
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.
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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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