<--- Back to Details
First PageDocument Content
Medical research / Clinical research / Pharmaceutical industry / Clinical trials / Clinical trial / Design of experiments / Drug discovery / Patient recruitment / Clinical trial portal / Academic clinical trial
Date: 2015-11-03 08:35:01
Medical research
Clinical research
Pharmaceutical industry
Clinical trials
Clinical trial
Design of experiments
Drug discovery
Patient recruitment
Clinical trial portal
Academic clinical trial

8 Best Practices for Site Identification I t’s important to start site identification as early as possible, and following best practices will ensure you find the right number of suitable sites for your study. Below a

Add to Reading List

Source URL: www.drugdev.com

Download Document from Source Website

File Size: 102,65 KB

Share Document on Facebook

Similar Documents

PLoS MEDICINE  CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts: Explanation and Elaboration Sally Hopewell1,2*, Mike Clarke1,3, David Moher4,5, Elizabeth Wager6, Philippa Middleton7

PLoS MEDICINE CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts: Explanation and Elaboration Sally Hopewell1,2*, Mike Clarke1,3, David Moher4,5, Elizabeth Wager6, Philippa Middleton7

DocID: 1qSLP - View Document

      Instructions to the Authors   The Editorial Process |  Clinical trial registry | Authorship Criteria |  Contribution Details |   Conflicts of Interest/ Competing Interests | Submission of Manuscripts |

     Instructions to the Authors   The Editorial Process |  Clinical trial registry | Authorship Criteria |  Contribution Details |   Conflicts of Interest/ Competing Interests | Submission of Manuscripts |

DocID: 1qEwn - View Document

      Instructions to the Authors   The Editorial Process |  Clinical trial registry | Authorship Criteria |  Contribution Details |   Conflicts of Interest/ Competing Interests | Submission of Manuscripts |

     Instructions to the Authors   The Editorial Process |  Clinical trial registry | Authorship Criteria |  Contribution Details |   Conflicts of Interest/ Competing Interests | Submission of Manuscripts |

DocID: 1qDUV - View Document

ASTRAZENECA GLOBAL POLICY GLOBAL PUBLICATIONS POLICY 1. PURPOSE This Global Policy applies to all publications originated or sponsored by

ASTRAZENECA GLOBAL POLICY GLOBAL PUBLICATIONS POLICY 1. PURPOSE This Global Policy applies to all publications originated or sponsored by

DocID: 1qDil - View Document

R48- Clinical trials methodology: key issues for successful study design and conduct a focussed workshop for Academic Clinical Trainees 1 JanuarySeptemberworkshop dateJuly 2014 London) Prof Jane B

R48- Clinical trials methodology: key issues for successful study design and conduct a focussed workshop for Academic Clinical Trainees 1 JanuarySeptemberworkshop dateJuly 2014 London) Prof Jane B

DocID: 1qCFb - View Document