Orphan Drugs in Canada: A “One Size Fits All” Regulatory Regime

Orphan Drugs in Canada: A “One Size Fits All” Regulatory Regime By Eileen McMahon and Denise Ramsden   Introduction Medicines targeting rare diseases, also known as orphan drugs,[1] once faced an uphill battle for research funding and market approval. The need for robust commercial incentives to create rare disease treatments spurred the establishment [...]

Orphan Drugs in Canada: A “One Size Fits All” Regulatory Regime2021-07-26T08:54:04-04:00

FDLI Annual Conference: Exploring Advanced Topics in Food and Drug Law

May 18–20, 2021 | Virtual Event

FDLI Annual Conference: Exploring Advanced Topics in Food and Drug Law2021-05-24T11:05:35-04:00

Summer Learning Series

The Summer Learning Series brings the top thinkers and leaders of our industry to speak on a broad array of topics essential to the food and drug law professional, covering matters that perhaps we all wish we knew a bit more about as we work and converse with clients, colleagues, and the FDA. Join [...]

Summer Learning Series2021-07-21T16:24:14-04:00

Pharmaceutical GMPs, Quality Control, and Data: A Deeper Look at FDA’s FY 2020 FDA Observations

Update Magazine | Summer 2021

Pharmaceutical GMPs, Quality Control, and Data: A Deeper Look at FDA’s FY 2020 FDA Observations2022-03-18T11:46:59-04:00

Author Happy Hour: Implementing Effective Escalation Processes in Life Sciences Companies

April 22, 2021 | 5:00 PM EDT | Virtual Event

Author Happy Hour: Implementing Effective Escalation Processes in Life Sciences Companies2021-04-23T11:03:11-04:00
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