{"product_id":"a-guide-for-clinical-research-professionals","title":"A Guide for Clinical Research Professionals","description":"\u003cp\u003eA Guide for Clinical Research Professionals covers the following topics: Overview of the Pharmaceutical Industry,  Drug Discovery and Drug Development , Pre-clinical studies, New Therapeutic Product - Regulatory Process Overview, Clinical trials - Fundamental elements, Ethical issues in Clinical research, International Conference on Harmonization and Good Clinical Practice, Institutional Review Board \/ Independent Ethic Committee (IRB\/IET): roles and responsibilities, Informed Consent Process, Overview of Some Clinical Trial Essential Documents, Data Collection in Clinical Trials, Investigator: Roles and Responsibilities. Investigator's Study File, Source Documents \u0026amp; Source Documents Verification (SDV), Clinical Data Validation Process \u0026amp; Query Management, Medical Data Coding \u0026amp; SAE Reconciliation, Statistical issues in clinical trials, Sponsor Definition, Sponsor-Company Responsibilities, Clinical Research Organizations, Clinical Research Associate (CRA)\/Clinical Monitor and other issues.\u003c\/p\u003e","brand":"BooksWholesale","offers":[{"title":"Paperback","offer_id":44275294961825,"sku":"9781105728709","price":92.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0462\/1120\/3233\/files\/1ynnzery-front-shortedge-384.jpg?v=1714080038","url":"https:\/\/bookswholesale.myshopify.com\/products\/a-guide-for-clinical-research-professionals","provider":"BooksWholesale","version":"1.0","type":"link"}