Regulatory Affairs for Medical Devices, Pharmaceuticals & Biologics

RA 101
Closed
Northeastern University
Boston, Massachusetts, United States
Partnership Development Coodinator
(7)
6
Timeline
  • July 18, 2022
    Experience start
  • July 19, 2022
    Project Scope Meeting
  • August 1, 2022
    Experience end
Experience
3/5 project matches
Dates set by experience
Preferred companies
Anywhere
Any
Any industries

Experience scope

Categories
Communications Operations Market expansion Product or service launch Sales strategy
Skills
regulatory affairs marketing medical devices regulatory sciences pharmaceuticals research commercialization
Learner goals and capabilities

A global, experiential, research university is seeking projects for their Master of Science in Regulatory Affairs capstone course. The Master of Science in Regulatory Affairs program is designed to both broaden and deepen the student’s understanding of current global compliance requirements and their practical application in the design, development, approval, and post marketing of products utilized within regulated industries.

The capstone course challenges students to exercise their ability to translate global regulatory requirements for globally regulated product commercialization into submission-ready documents and broadly applicable regulatory science solutions.

This is your opportunity to connect with students and faculty from a renowned institution in New England that consistently ranks among the top universities in the United States and is known for its focus on interdisciplinary education, extensive research output, and collaborative student culture.

Learners

Learners
Graduate
Any level
80 learners
Project
40 hours per learner
Learners self-assign
Teams of 5
Expected outcomes and deliverables

Deliverables are negotiable, and will seek to align the needs of the students and the organization.

Some final project deliverables might include:

  1. A 10-15 minute presentation on key findings and recommendations
  2. A detailed report including their research, analysis, insights and recommendations
Project timeline
  • July 18, 2022
    Experience start
  • July 19, 2022
    Project Scope Meeting
  • August 1, 2022
    Experience end

Project Examples

Requirements

Student teams will work with your organization to identify your needs and provide actionable recommendations, based on in-depth research and analysis.

Desired project topics include:

Strategic Regulatory Affairs

  • Classification
  • Combination Product Approvals
  • Global Commercialization

Clinical Research

  • Clinical Trial Design
  • Clinical Operations
  • Study Rationales

Regulatory Compliance

  • Adverse event profiling
  • REMS
  • Post Market Surveillance

General Regulatory Affairs

  • Regulatory Market Research

We invite you to share your projects for consideration. Please include an executive summary of the regulatory affairs problem or topic. Be sure to include a brief description of your organization and mission.

We are also seeking projects for many other academic domains including, Communications, Marketing, Public Policy and General Business. Please reach out for more details!

Additional company criteria

Companies must answer the following questions to submit a match request to this experience:

  • Q - Checkbox
  • Q - Checkbox