Introduction - Consulting / Training Services

ICH-GCP E6 (R2) ‘2.0 Principles’ – Section 2.3 states: “The rights, safety, and well-being of the trial subjects are the most important considerations and should prevail over interests of science and society”.

To achieve the highest standards of subject protection in the field of clinical research requires the implementation of the highest standards in the design, development, delivery, and follow-up of all aspects of clinical trial conduct. In turn, the foundation for delivering high quality clinical trials is the design, development, delivery and follow-up of appropriate training sessions targeting the multiple roles engaged in clinical trial conduct. The ACROSS Global Training Academy prides itself in providing thoughtful, engaging and practical training sessions to allow individuals involved in all aspects of clinical trial conduct to fulfil their duties and to meet the requirements of GxP guidance as well as international regulations.

Our Goal

Our goal is to ensure the highest quality and standards of our training courses (in terms of both content and delivery) to help ensure that each individual involved in conducting a trial has received the appropriate quality of training for them to perform their respective task(s) (ICH-GCP E6 (R2) 2.0 Principles – Section 2.8).

Unparalleled, Comprehensive Training Module / Course Design

Each ACROSS Global Training Academy module / course has been meticulously designed to ensure the best possible learning outcome for our attendees. Our modules / courses include:

  • Clear, well-spoken, English speaking presenters for international attendees.
  • Clear, concise module / course objectives.
  • High-level module / course ‘Content Overview’.
  • Consistent ‘signposting’ ensuring easy-to-follow content.
  • Key words and statements clearly highlighted.
  • Relevant sections of Good Clinical Practice appropriately referenced.
  • Embedded quizzes – focused on reinforcing key learning outcomes.
  • Ample time to address attendee questions throughout the module / course.
  • Summary section to review objectives and address attendee clarifications.
  • Feedback section for first-hand feedback from attendees.
  • Reference section for additional information / documents.

Training Instructors

To achieve the highest standards of subject protection in the field of clinical research requires the highest standards in the design, development, delivery, and follow-up of training courses. Our Training Instructors have a wealth of experience in conducting Clinical Trials as well as outstanding skills in delivering training in a meaningful, understandable and engaging manner for the audience.

Training Instructor Profiles

Training Delivery Modalities

ACROSS Global offers the entire spectrum of training delivery modalities, including e-Learning, Instructor-Led-Training (ILT) [both online and classroom], Scheduled Webinars as well as On-Demand Webinars. We specialize in custom-tailored training courses to meet the specific needs of our clients.