Training & Events

Postgraduate Course Clinical Pharmacology Drug Development Regulation

The longest-running professional development program providing a holistic overview of the global drug development landscape and what it takes to bring a new drug or biologic to market.

Frequency: Annual

Postgradute Course in Clinical Pharmacology, Drug Development & Regulation

2026 Tufts CSDD | 53rd Annual

The longest-running professional development program providing a holistic overview of the global drug development landscape and what it takes to bring a new drug or biologic to market.

Course Information TBD

ABOUT THIS COURSE:


The Tufts CSDD Postgraduate Course in Clinical Pharmacology, Drug Development and Regulation is the longest-running professional development program in the biopharma space. Now in its 53rd year, this unique annual course prepares both new and experienced drug developers, regulators, policy makers, clinical investigators, and academic researchers for success in the life-sciences sector. Thousands of drug development professionals are alumni of this prestigious one-of-a-kind program. Top speakers from industry, academia, and the FDA share their expertise to create a highly stimulating and rewarding learning environment. For a complete list of topics and speakers, download the course brochure below.

The goal of the course is to provide a comprehensive overview of the pharmaceutical development process, focusing on topics vital to professionals involved in all aspects of bioinnovation. Participants include individuals employed by pharmaceutical and biotechnology companies, regulatory agencies, academic institutions, government entities, outsourcing providers, consultancies, investment firms, and other biopharmaceutical organizations involved in the research, development, regulation, and marketing of pharmaceutical products.

Educational Objectives

Clinical Pharmacology: Integrate the relevant pharmacology, pharmacokinetics, and statistics related to drug development and the nature of evidence required for proof of efficacy and safety.

Drug Development & Clinical Trials: Using a case-study approach, identify and solve practical, theoretical, and technical problems in human drug studies and analyze an experimental design for a new drug candidate.

Regulation: Evaluate the science, laws, and regulations pertaining to the development and review of new drug products in the U.S., Europe, Japan & other pharmaceutical markets.

2026 Course Dates Coming Soon
 

2019 Postgraduate Course Attendees - Who Should Attend

WHO SHOULD ATTEND?

Professionals working in or with the research-based biopharmaceutical industry 

Physicians, clinical investigators, pharmacists, nurses, and academic researchers 

Regulators and other government agencies involved in drug development 

Outsourcing providers, consultants, investors, and analysts

Tuft CSDD Credly Course Completion Badge

EARN A DIGITAL COURSE COMPLETION BADGE & CERTIFICATE!

Showcase the knowledge and skills you acquired from the program.

Share your learning achievements with clients, employers, and colleagues on online platforms and social media networks like LinkedIn, Facebook and X

“ The mock drug groups activity was very helpful because it brought together a handful of people from different backgrounds and professions. It encouraged team-building and communication — two things that are very much needed in the work field. ”
Past Participant
“ Taking the Tufts course was a tremendously beneficial experience for me. I’m so grateful to have learned so much and met such wonderful colleagues. You created a fantastic roster of speakers and presentations. ”
Past Participant
“ Being new to the industry, I appreciated that all the presentations provided excellent background information before examining each topic in more depth. ”
Past Participant
“ The professors are incredibly experienced and knowledgeable. Classes covered foundational and advanced concepts while integrating real-world strategies that I could apply immediately to my responsibilities within Scientific & Medical Affairs. ”
Past Participant
“ With 20 years of experience in the drug product development industry, primarily focused on clinical trial materials, I found this course to be incredibly beneficial. It added immense value not only to my personal growth but also to my peers, clients, and ultimately the patients we serve. I thoroughly enjoyed the course and only wish I had taken it sooner! ”
Past Participant
Regular Rate
$2,750
Circle of Supporter Sponsor Rate
$2,450
Academic, Nonprofit, & Govt Rate
$2,450

The postgraduate program typically receives 125 - 150 participants. Many companies choose to send multiple staff to participate in the program under a special, discounted registration rate. If you would like to learn more about registering a group, please contact Sarah Wrobel at @email

 

Get More Information

Have questions or want to register? Fill out the below form to connect with our enrollment team