This training series is designed to foster both personal and professional growth for clinical research professionals. It focuses on enhancing leadership, communication, time management, and problem-so
This course emphasizes the importance of creating and maintaining a safe work environment within clinical research settings. It covers critical topics such as hazard identification, risk assessment, a
Focused on the meticulous process of preparing application files for clinical research, this training equips professionals with the knowledge to assemble comprehensive and compliant documentation. Par
This course is essential for understanding how to detect, document, and report adverse events (AEs) and serious adverse events (SAEs) in clinical trials. It covers the regulatory requirements for AE/S
A comprehensive introduction to the fundamental principles of clinical research, this orientation is designed for new employees or those unfamiliar with the clinical research field. It covers the role
With a focus on data privacy and protection, this training ensures that clinical research professionals are fully compliant with the General Data Protection Regulation (GDPR). Participants learn about
This training is aimed at preempting potential regulatory issues in clinical trials. Participants are trained on the importance of proactive planning, risk assessment, and implementing preventive meas
This training program delves into the intricacies of clinical trial data management. Participants learn best practices for entering, verifying, and maintaining high-quality data, as well as techniques
This training is designed to equip site managers and coordinators with the skills necessary to oversee clinical trial sites efficiently. Topics covered include site setup, staff coordination, budget m
Tailored to the specific needs of individual projects, these medical trainings ensure that clinical research staff have the in-depth medical knowledge required for the trial they are working on. Wheth
This training ensures that all personnel are thoroughly familiar with ATAŞEHIR CRO's internal Standard Operating Procedures (SOPs). Participants will gain a comprehensive understanding of the process
Effective documentation is the cornerstone of successful clinical research, and this training focuses on the best practices for maintaining accurate, comprehensive, and compliant records. Participants
This course is essential for clinical research associates and monitors, covering the principles and practices of effective trial monitoring. Participants learn how to ensure that clinical trials are c
This specialized training addresses the regulatory landscape for clinical trials involving medical devices. Participants will gain a thorough understanding of the unique requirements for device trials
Focusing on the regulatory framework governing pharmaceutical and biological product trials, this training provides participants with a deep understanding of the legal and ethical standards required f
This comprehensive GCP training ensures that all clinical research professionals are well-versed in the international ethical and scientific quality standards for designing, conducting, recording, and
