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thincpharm.com

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

THinc is a pharmaceutical regulatory affairs, medical writing, and nonclinical safety consulting company that provides an integrative approach to consulting throughout the drug-development process.

http://www.thincpharm.com/

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CONTACTS AT THINCPHARM.COM

Debra Hathaway

350 Seco●●●●●●●● Suite 9

Los●●●tos , California, 94022

United States

1.65●●●●7346
de●●●●●●●●●●●●@thincpharma.com

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Debra Hathaway

350 Seco●●●●●●●● Suite 9

Los●●●tos , California, 94022

United States

1.65●●●●7346
de●●●●●●●●●●●●@thincpharma.com

View this contact

Debra Hathaway

350 Seco●●●●●●●● Suite 9

Los●●●tos , California, 94022

United States

1.65●●●●7346
de●●●●●●●●●●●●@thincpharma.com

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THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services | thincpharm.com Reviews
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THinc is a pharmaceutical regulatory affairs, medical writing, and nonclinical safety consulting company that provides an integrative approach to consulting throughout the drug-development process.
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1 advisory committee
2 annual reports
3 approval
4 FDA audit
5 Bay Area
6 biopharmaceutical
7 chemistry
8 biological license application BLA
9 clinical monitors
10 clinical report
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about thinc,therapeutic areas,newsreel,legal/privacy,regulatory affairs,strategies,regulatory applications,interactions with agencies,project management,operations,medical writing,writing capabilities,regulatory documents,clinical documents,useful links
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THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services | thincpharm.com Reviews

https://thincpharm.com

THinc is a pharmaceutical regulatory affairs, medical writing, and nonclinical safety consulting company that provides an integrative approach to consulting throughout the drug-development process.

INTERNAL PAGES

thincpharm.com thincpharm.com
1

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

http://www.thincpharm.com/WRregulatory.html

Our Vision and Values. Chemistry, Manufacturing, Controls. Product Development and Planning. Data Interpretation, Preparation, and Review. US Drug Development: The IND Submission. IND Overview for a First-in-Human Trial. Before the IND Application. THinc . . . a REGULATORY AND MEDICAL WRITING DEPARTMENT. For clients who need to prepare regulatory, clinical, and scientific documents, we can help you develop and write documents with consistent key messages from concept through completion.

2

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

http://www.thincpharm.com/newsreel.html

Our Vision and Values. Chemistry, Manufacturing, Controls. Product Development and Planning. Data Interpretation, Preparation, and Review. US Drug Development: The IND Submission. IND Overview for a First-in-Human Trial. Before the IND Application. Our Vision and Values. Therapeutic Areas of Expertise. Newsreel - What's New at THinc. NEW SERVICE - Clinical Operations. Recent Assignments FY 2012 - Gap Analyses and Strategies. Strategic plans Strategized with clients on development plans for products in at...

3

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

http://www.thincpharm.com/NCSnonclinical.html

Our Vision and Values. Chemistry, Manufacturing, Controls. Product Development and Planning. Data Interpretation, Preparation, and Review. US Drug Development: The IND Submission. IND Overview for a First-in-Human Trial. Before the IND Application. THinc . . . a NONCLINICAL SAFETY DEPARTMENT. Product Development and Planning. Data Interpretation, Preparation, and Review. Prepare customized protocol outlines with key study requirements. Obtain proposals from contract research laboratories.

4

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

http://www.thincpharm.com/WRclinical.html

Our Vision and Values. Chemistry, Manufacturing, Controls. Product Development and Planning. Data Interpretation, Preparation, and Review. US Drug Development: The IND Submission. IND Overview for a First-in-Human Trial. Before the IND Application. THinc . . . a REGULATORY AND MEDICAL WRITING DEPARTMENT. For clients who need to prepare regulatory, clinical, and scientific documents, we can help you develop and write documents with consistent key messages from concept through completion.

5

THinc pharmaceutical regulatory consulting, medical writing, and nonclinical safety services

http://www.thincpharm.com/THincRegulatory.html

Our Vision and Values. Chemistry, Manufacturing, Controls. Product Development and Planning. Data Interpretation, Preparation, and Review. US Drug Development: The IND Submission. IND Overview for a First-in-Human Trial. Before the IND Application. THinc . . . a REGULATORY AFFAIRS DEPARTMENT. For clients who need regulatory affairs support, we can help you strategize, formulate, and develop solutions to regulatory issues and prepare and process submissions that are compliant with regulatory guidelines.

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