# Book CeDeWu — Zwinne zarządzanie projektami badań klinicznych (Polish) — CeDeWu 69304A02077KS

**URL:** https://aio.lv/en/product--cedewu-69304a02077ks--11903543
**Data updated:** 2026-03-10 00:39 (EET)
**Category:** Textbooks & Study Guides
**Manufacturer:** CeDeWu
**Manufacturer code:** 69304A02077KS
**EAN:** 9788381026352
**Warranty:** 2 Years
**Availability:** Out of stock

## Summary description

A Polish-language professional book from CeDeWu covering agile management of clinical research projects. Focuses on methods, processes and tools for implementing agile frameworks in clinical trials, risk management, team roles and documentation. Useful for clinical project managers, research coordinators and healthcare professionals involved in trial planning and execution.

## Long description

Book CeDeWu — Zwinne zarządzanie projektami badań klinicznych is a Polish-language professional guide published by CeDeWu that presents principles and practical approaches to applying agile management in clinical research projects. The book explains methods, processes and tools for adapting agile frameworks to the specific requirements of clinical trials, including planning, risk assessment, documentation and team collaboration. It is intended for professionals responsible for designing, coordinating and overseeing clinical studies who need a structured reference on integrating agile practices into regulated environments.
Advantages
This CeDeWu publication provides a focused examination of agile methodologies tailored to clinical research contexts, combining theoretical foundations with practical examples. The content addresses risk identification and mitigation, role definitions within multidisciplinary teams, and documentation practices compatible with regulatory expectations. The book serves as a concise resource for learning how to streamline project workflows while maintaining compliance and data integrity.
Suitable for
 Clinical project managers seeking agile techniques applicable to trials
 Research coordinators and clinical operations staff involved in study execution
 Healthcare professionals and scientists participating in trial planning
 Quality assurance and regulatory affairs specialists interested in process adaptation
Key specifications
 Language: Polish
 Format: Professional non-fiction book focused on management methods
 Main topics: Agile frameworks, project processes, risk management, team roles, documentation
 Audience: Clinical research professionals and study coordinators
How to use
Use the book as a reference during project planning and at key stages of a clinical trial to inform the design of workflows, define team responsibilities and develop documentation templates. Read chapters that correspond to immediate needs—such as risk management or team roles—and apply suggested tools and process steps to existing procedures. Combine theoretical sections with practical examples to adapt recommendations to the organization’s size, trial phase and regulatory context.
Usage recommendations
Consult the book alongside local standard operating procedures and regulatory guidance; adapt agile practices incrementally and validate changes through pilot projects before wider implementation in clinical programs.

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