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| Available: 0 |
| List Price:$79.00 |
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| Edition: | 3rd |
| Publisher: | CenterWatch, Inc. |
| ISBN: | 1-930624-60-3 (1930624603) |
| ISBN-13: | 978-1-930624-60-3 (9781930624603) |
| New Edition: | 1-930624-73-5 |
| Binding: | Softcover |
| Copyright: | 2011 |
| Publish Date: | 07/11 |
| Weight: | 2.36 Lbs. |
| Pages: | 664 |
| Carton Quantity: | 16 |
| Subject Class: | PHM (Pharmacy and Pharmaceutical Industry) |
| Remarks: | A New Edition of this Title is Available |
| Return Policy: | Non-Returnable. |
| Table Of Contents: |
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| Discipline: | Pharmacology | | Subject Definition: | Clinical Trials as Topic-Standards; Drug Approval-Org & Adm | | NLM Class: | QV 771 | | LC Class: | RM301.27 | | Abstract: | The CRA's Guide to Monitoring Clinical Research, now in its third edition, continues to be a key resource for both novice and experienced CRAs seeking to learn more about the field of monitoring or to better understand their roles and responsibilities as the industry becomes more global and technologically focused. With helpful tips and strategies, checklists, personal experiences, key takeaways and exercises, plus new chapters on clinical trial roles and responsibilities, monitoring for device and biologic trials, globalization of studies, EDC and more, The CRA's Guide is a must-have training and educational tool that you ll refer to again and again....Recommended for: -Novice and experienced CRAs: Health professionals interested in pursuing a career as a study monitor. Instructors conducting training and educational programs. |
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