{"product_id":"the-cras-guide-to-monitoring-clinical-research","title":"The CRA's Guide to Monitoring Clinical Research","description":"\u003cp\u003eThe CRAs Guide to Monitoring Clinical Research is a valuable and practical educational resource for the individual readers and for group and staff training programs. Written by Karen E. Woodin  Ph.D.  and John C. Schneider  this 400 page CE-accredited book is an ideal resource for novice and experienced CRAs  as well as professionals interested in pursuing a career as study monitors. The CRAs Guide explains the role and responsibilities of a CRA  informs readers of the history of the regulations  explains in detail the research process and describes the regulations and GCPs that govern clinical research. Book topics: - Preparing for a study and selecting investigators - Obtaining and monitoring informed consent - Preparing for a monitoring visit - Recruiting and retaining study subjects - Conducting adverse event and safety monitoring - Preparing for audits and detecting fraud\u003c\/p\u003e","brand":"My Store","offers":[{"title":"Default Title","offer_id":44946968510517,"sku":"ByrdShop_1930624379","price":39.98,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0627\/8139\/0901\/files\/9781930624375.jpg?v=1769975168","url":"https:\/\/atxbooks.com\/products\/the-cras-guide-to-monitoring-clinical-research","provider":"ATX Books","version":"1.0","type":"link"}