Meredith Brown-Tuttle
Executive Director, Regulatory Affairs at Crinetics Pharmaceuticals | San Jose, California, United States
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Meredith Brown-Tuttle serves as the Chief Regulatory Strategist at Regulatorium, where she leverages her extensive global regulatory affairs experience spanning over 32 countries. In her current role, Meredith is instrumental in shaping and executing comprehensive regulatory strategies for a diverse portfolio of drugs, medical devices, and combination products. Her expertise in regulatory intelligence is pivotal, as she conducts in-depth regulatory research and intelligence gathering across various therapeutic indications, ensuring that her clients are well-informed and strategically positioned in the ever-evolving regulatory landscape.
One of Meredith's key projects involves the development and management of global regulatory strategies that facilitate successful submissions, including Investigational New Drug (IND) applications, New Drug Applications (NDA), and Marketing Authorization Applications (MAA). Her ability to perform strategic gap analyses allows her to identify potential regulatory hurdles early in the development process, thereby mitigating risks and enhancing the likelihood of successful outcomes. Meredith's proactive approach to regulatory agency interactions—both within the U.S. and internationally—has proven invaluable to Fortune 500 companies seeking to navigate complex regulatory environments.
In addition to her strategic oversight, Meredith is adept at coordinating research submissions and responses to regulatory agencies, ensuring compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOP). Her skills in pharmacovigilance and Clinical Research Organization (CRO) management further bolster her capability to support clients through the intricacies of regulatory requirements. With a keen eye for detail and a commitment to excellence, Meredith Brown-Tuttle continues to be a driving force in advancing regulatory strategies that align with the dynamic needs of the healthcare industry.
Executive Director, Regulatory Affairs at Crinetics Pharmaceuticals in March 2025 to Present
Chief Regulatory Strategist at Regulatorium in March 2007 to March 2025
Board Member at The Alliance for Artificial Intelligence in Healthcare (AAIH) in February 2022 to May 2023
Vice President, Regulatory Affairs at Recursion in April 2021 to September 2022
VP, Regulatory & Quality at Lyric Pharmaceuticals, Inc. in July 2015 to July 2018
Instructor, Regulatory Affairs at UCSC Extension in Silicon Valley in January 2005 to December 2015
Author/Instructor at Barnett Educational Services in February 2009 to February 2015
Director, Regulatory Affairs at APT Pharmaceuticals in February 2008 to July 2010
Manager, Regulatory Affairs at PDL BioPharma, Inc. in January 2005 to January 2007
Associate Director, Regulatory at Clinimetrics in January 2005 to January 2005
Manager, Regulatory Affairs at NeurogesX, Inc. in January 2002 to January 2004
Regulatory Associate at Oculex in January 2000 to January 2002
Clinical Research Associate at ORATEC Interventions, Inc. in January 1999 to January 2000
Data Management at RBI/IBAH in January 1996 to January 1997
Research Assistant at Vitaphore in January 1991 to January 1992
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Regulatory Strategy
Regulatory Interactions
Digital Strategy
Pharmaceutics
Regulatory Research
Regulatory Affairs
FDA
IND
Regulatory Submissions
Regulatory intelligence
Marketing Applications
NDA
Clinical Trials
Articles
Clinical Development
GCP
Biotechnology
Pharmaceutical Industry
Drug Development
eCTD
Oncology
Medical Writing
Regulatory Requirements
Sop
Medical Devices
Clinical Research
Biopharmaceuticals
MAA
Infectious Diseases
Protocol
Electronic Submissions
Biologics
Regulatory Documentation
Clinical Study Design
Neuroscience
Clinical Data Management
Regulatory Guidelines
ICH-GCP
Regulatory Intelligence
Regulations
CRO
SOP
Pharmacovigilance
Life Sciences
CRO Management
Good Clinical Practice (GCP)
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
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Discover more about Crinetics PharmaceuticalsWhat is Meredith Brown-Tuttle email address?
Email Meredith Brown-Tuttle at [email protected]. This email is the most updated Meredith Brown-Tuttle email found in 2026.
How to contact Meredith Brown-Tuttle?
To contact Meredith Brown-Tuttle send an email to [email protected].
What company does Meredith Brown-Tuttle work for?
Meredith Brown-Tuttle works for Crinetics Pharmaceuticals
What is Meredith Brown-Tuttle's role at Crinetics Pharmaceuticals?
Meredith Brown-Tuttle is Executive Director, Regulatory Affairs
What is Meredith Brown-Tuttle's Phone Number?
Meredith Brown-Tuttle's phone (213) ***-*247
What industry does Meredith Brown-Tuttle work in?
Meredith Brown-Tuttle works in the Hospitals And Health Care industry.
Meredith Brown-Tuttle Email Addresses
Meredith Brown-Tuttle Phone Numbers
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