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JCRPM LLC

  • The US FDA Agent Source

  • Effortless HR Solutions for Your Clinical Study

 

JCRPM LLC works in close partnership with our clients to look to ensure regulatory and development success throughout the early drug product lifecycle.

Our 
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Get to Know Us

JCRPM LLC provides an early Regulatory Solution for its Sponsors as part of their drug development process, focusing on Sponsor satisfaction. JCRPM LLC helps Sponsors manage clinical study workflows. Through its multi-disciplinary expertise, JCRPM LLC will bring together best practices in the execution of an early drug product development.

Events Source

FDA | Virtual:

 

Model Master Files: Advancing Modeling and Simulation in Generic Drug Development and Regulatory Submissions

 

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March 13, 2025

Our Services

1

FDA Submissions

Pre-IND Meeting

IND Application

ODD Application

2

IND Lifecycle Support

Through early-stage development of your product, we can assist with all your regulatory needs across the early clinical studies of your products.

3

Project Management

We provide program management support for early-stage drug development programs.

Get in Touch

13822 Harrier Way 

Clarksburg, MD 20871

979-220-7853

jcho@jcrpmllc.com

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