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Are you a statistical programmer in the pharmaceutical industry looking to enhance your skills and comply with regulatory requirements? Look no further! Our comprehensive guide "Creating Standardized Clinical Trial Data with SAS" is here to support you every step of the way. Learn the essential concepts, industry knowledge, and SAS programming practices necessary to create standardized clinical data aligned with CDISC rules. Take your programming skills to the next level and ensure compliance with ease.
Unlock the secrets of standardized clinical data creation with our easy-to-follow and practical book. Discover how to structure data effectively, from annotating eCRFs to defining relationships between SDTM and ADaM. Our book provides a step-by-step approach, complete with clear explanations and example code, making complex concepts simple to grasp. With our guidance, you'll develop the confidence and skills required to excel in creating standardized clinical trial data that meets industry standards.
Don't miss out on this opportunity to advance your career in the pharmaceutical industry. Whether you're a novice programmer or looking to refresh your knowledge, this book is the perfect resource to elevate your skills and stay ahead of the curve. Equip yourself with the tools and knowledge needed to succeed in creating compliant clinical trial data. Get your hands on "Creating Standardized Clinical Trial Data with SAS" today!
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