Our training programs are designed to provide hands-on experiences and realistic simulations that prepare physicians and healthcare professionals to face any challenge in their daily practice.
With us, you won’t just gain theoretical knowledge—you’ll develop practical skills that make a real difference in your career.

 

  • Stress Management & Professional Wellbeing
  • Teamwork & Leadership
  • Technology & Telemedicine
  • Research & Evidence-Based Practice
  • Patient-Centered Care

 

Research & Evidence-Based Practice

  • Introduction to Clinical Research
  • Protocol structure
  • Clinical trial lifecycle

  • ICH-GCP principles
  • Responsibilities of investigators and sponsors
  • Subject protection and essential document management

  • Ethical and legal consent procedures
  • Document requirements and effective communication
  • Version control, updates, and signature management

  • Receipt, storage, and handling conditions
  • Traceability, preparation, and administration
  • Documentation and returns

  • Proper completion of CRFs/eCRFs
  • Validation, queries, and database lock
  • Data confidentiality and protection

  • Identification and reporting of adverse events (AEs/SAEs).
  • Forms and reporting timelines
  • Causality assessment and follow-up

  • National and international legislation
  • Required documentation for study approval
  • Liaison with regulatory agencies (AEMPS, EMA, FDA)

  • CRA roles and visit types (initiation, monitoring, close-out)
  • Source data verification (SDV) and deviation resolution
  • Audit and inspection readiness

  • Training in specific systems (Medidata, RedCap, etc.)
  • Secure access, user roles, and platform navigation
  • Proper logging and traceability

  • Guided practice: screening, enrollment, interim, and close-out visits
  • Patient interaction, timing, and documentation
  • Simulated cases to reinforce learning

  • Full site management: logistics, scheduling, and visit coordination
  • Collaboration with monitors, labs, and pharmacy
  • Handling deviations, inspections, and reporting
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