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Cambridge Healthtech Institute - Market Research Reports

Cambridge Healthtech Institute (CHI) is the preeminent life science network for leading researchers and business experts from top pharmaceutical, biotech and academic organizations. CHI’s portfolio of products includes Cambridge Healthtech Institute Conferences, Insight Pharma Reports, Cambridge Marketing Consultants, Barnett International, Cambridge Meeting Planners and Healthtech Publishing, which includes Bio-IT World, Clinical Informatics News and Diagnostics World.

1 Year - U.S. Regulatory Reporter Newsletter for Addresses in Europe - Product Thumbnail Image

1 Year - U.S. Regulatory Reporter Newsletter for Addresses in Europe

  • Newsletter
  • December 2024
  • United States, Europe United States, Europe
U.S. Regulatory Reporter Newsletter for Addresses in North America - Product Thumbnail Image

U.S. Regulatory Reporter Newsletter for Addresses in North America

  • Newsletter
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1 Year - U.S. Regulatory Reporter Newsletter for International Addresses Outside of Europe - Product Thumbnail Image

1 Year - U.S. Regulatory Reporter Newsletter for International Addresses Outside of Europe

  • Newsletter
  • December 2024
  • United States, Europe, ... United States, Europe, Global
HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014 - Product Thumbnail Image

HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014

  • Book
  • April 2014
  • United States
The US Drug Approval Trends and Yearbook 2008/2009 - Product Thumbnail Image

The US Drug Approval Trends and Yearbook 2008/2009

  • Book
  • July 2008
  • 200 Pages
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State-by-State Clinical Trial Requirements Reference Guide 2012 - Product Thumbnail Image

State-by-State Clinical Trial Requirements Reference Guide 2012

  • Book
  • November 2012
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Medical Device Development: Regulation and Law 2014 - Product Thumbnail Image

Medical Device Development: Regulation and Law 2014

  • Book
  • June 2014
  • 600 Pages
Biologics Development: A Regulatory Overview 3rd Edition (2004) - Product Thumbnail Image

Biologics Development: A Regulatory Overview 3rd Edition (2004)

  • Book
  • January 2004
State-by-State Clinical Trial Requirements Reference Guide - Product Thumbnail Image

State-by-State Clinical Trial Requirements Reference Guide

  • Book
  • September 2006
  • 200 Pages
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors - Product Thumbnail Image

The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors

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  • 134 Pages
CFR/ICH GCP Reference Guide for Medical Devices 2020 - Product Thumbnail Image

CFR/ICH GCP Reference Guide for Medical Devices 2020

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  • January 2020
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Biopharmaceutical R&D Statistical Sourcebook 2018/2019 - Product Thumbnail Image

Biopharmaceutical R&D Statistical Sourcebook 2018/2019

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  • April 2018
  • 486 Pages
New Drug Approval in the European Union - Product Thumbnail Image

New Drug Approval in the European Union

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  • June 2002
  • 356 Pages
  • Europe
Medical Device Development: Regulation and Law, All New Edition! - Product Thumbnail Image

Medical Device Development: Regulation and Law, All New Edition!

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  • September 2009
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HIPAA and Human Subject Research: A Question and Answer Reference Guide - Product Thumbnail Image

HIPAA and Human Subject Research: A Question and Answer Reference Guide

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  • January 2003
  • 139 Pages
CRA Training Series: A 7-Volume CRA Self-Study Curriculum - Product Thumbnail Image

CRA Training Series: A 7-Volume CRA Self-Study Curriculum

  • Book
  • September 2018
  • 16 Results (Page 1 of 1)
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