Our Services

  1. Anasayfa
  2. Our Services

Supply of Qualified Clinical Research Personnel

  • Senior Clinical Research Specialist
  • Clinical Research Associate (CRA)
  • Clinical Research Specialist
  • Field Manager
  • Project Manager
  • Regulatory Submission Specialist
  • SIP Support Specialist
  • Contract Specialist
  • Country Clinical Trials Assistant
  • Data Entry Support Personnel
  • Initial Submission and Activation Lead
  • Financial CTA
  • Clinical Research Nurse
  • Medical Translator
  • Personnel for Other Relevant Positions in Clinical Research Based on Your Needs

Görsel-Supply of Qualified Clinical Research Personnel
Görsel-Pharmaceutical and Non-Pharmaceutical Clinical Trials

Pharmaceutical and Non-Pharmaceutical Clinical Trials

  • Phase 2-4 Clinical Trials
  • Early Access Programs
  • Observational Studies (Cross-Sectional, Retrospective, and Prospective)
  • Medical Device Studies

Trainings

  • Investigator Meeting
  • Monitor and Investigator Trainings
  • Good Clinical Practices (GCP) and Current Regulations Training
  • Advanced Good Clinical Practices (GCP)
  • CRA School
  • Basic CRA Trainings
  • Site Organization Management in Clinical Trials
  • Statistics Training
  • Medical Statistics Training
  • Basic Medical Statistics Training
  • Advanced Medical Statistics Training

Görsel-Trainings
Görsel-Support Services

Support Services

  • Patient Support Program
  • Site Support Service
  • Medical Consulting
  • IWR Systems

Medical Software

  • Protocol Writing
  • Case Report Form (CRF) and Electronic Case Report Form (eCRF) Design
  • Informed Consent Form (ICF) Design
  • Article
  • Poster
  • Clinical Study Final Report
  • Clinical Study Protocol and Amendments
  • Abstract
  • Synopsis

Görsel-Medical Software
Görsel-Regulatory Authority Submissions

Regulatory Authority Submissions

In Your Pharmaceutical and Non-Pharmaceutical Clinical Trials:

  • Preparation, Submission, Delivery, Follow-up, and Reporting of the Initial Application File to the Ethics Committee and the Turkish Medicines and Medical Devices Agency (TMMDA)
  • Ethics Committee and Turkish Medicines and Medical Devices Agency (TMMDA) Submission Support Throughout the Clinical Research Process (Including Amendment and Significant Amendment Applications)

Data Management & Statistics

  • Validation and Query Management
  • Database Preparation
  • Data Entry
  • Case Report Form (CRF) and Electronic Case Report Form (eCRF) Preparation
  • CRF and eCRF User Guide
  • Double Data Entry
  • Data Management
  • Development of Data Management Plan (DMP) and Statistical Analysis Plan (SAP)
  • Sample Size Calculation
  • Randomization
  • Statistical Analysis Plan
  • Interim Statistical Analysis
  • Final Statistical Analysis

Görsel-Data Management & Statistics
Görsel-Therapeutic Areas

Therapeutic Areas

  • Endocrinology
  • Infectious Diseases
  • Physical Therapy and Rehabilitation
  • Gastroenterology
  • Pulmonology
  • Hematology
  • Cardiology
  • Nephrology
  • Neurology
  • Ophthalmology
  • Oncology
  • Pathology
  • Psychiatry

Clinical Trials

  • Feasibility Assessments
  • Site and Investigator Selection
  • Site Initiation and Close-Out Visits
  • Monitoring
  • Co-Monitoring
  • Study Materials Inventory
  • Clinical Research Associate (CRA) Support
  • Data Entry Support Personnel
  • Project Management
  • Site Management
  • Interactive Voice/Web Response Systems (IXRS, IVRS, IWRS)
  • Patient Recruitment
  • Newsletter
  • Audit/Compliance
  • Ethics Committee and Ministry of Health Applications

Görsel-Clinical Trials