ASCEND BY NTHRYS
Research Abroad Products

Clinical Trials Workshops

Click a category to proceed further.

Showing 1–12 of 50 categories
GCP Compliance and Regulatory Framework
Master Good Clinical Practice guidelines, regulatory standards, and audit procedures for clinical trial professionals seeking compliance certification.
3+WORKSHOPS
PROGRAMMES
ICH GCP Guidelines Implementation and Protocol Compliance IND and CTA Submission Strategy for Regulatory Success Quality Overall Summary and Module 2 ECTD Preparation +2 more programmes
Explore workshops →
Electronic Data Capture Systems Training
Learn industry-standard EDC platforms, data entry protocols, and digital documentation workflows for clinical research coordinators and data managers.
3+WORKSHOPS
PROGRAMMES
Advanced EDC Database Design and Architecture EDC Form Building and Validation Rules Implementation Real-Time EDC Data Quality and Audit Trail Management +2 more programmes
Explore workshops →
Informed Consent Process and Documentation
Train on ethical consent procedures, participant communication, and proper documentation for clinical trial coordinators and site staff.
3+WORKSHOPS
PROGRAMMES
ICF Document Compliance and Regulatory Mapping Readability Assessment and Plain Language Optimization Electronic Consent Technology Implementation and Validation +2 more programmes
Explore workshops →
Adverse Event Reporting and Pharmacovigilance
Develop expertise in safety monitoring, serious adverse event reporting, and post-market surveillance for safety and clinical staff.
3+WORKSHOPS
PROGRAMMES
MedDRA Coding and Standardization in Pharmacovigilance Serious Adverse Event Assessment and Causality Evaluation Safety Database Management and eCTD Submission Workflows +2 more programmes
Explore workshops →
Protocol Development and Study Design
Master clinical trial protocol creation, statistical design, and study methodology for research scientists and protocol managers.
3+WORKSHOPS
PROGRAMMES
ICH-GCP Compliance and Protocol Amendment Management Statistical Randomization Strategies and Blinding Techniques Inclusion and Exclusion Criteria Development for Trials +2 more programmes
Explore workshops →
Subject Recruitment and Retention Strategies
Build practical skills in patient identification, enrollment strategies, and retention techniques for site coordinators and recruitment specialists.
3+WORKSHOPS
PROGRAMMES
Eligibility Screening and Patient Stratification Protocols Subject Retention Analytics and Dropout Risk Mitigation Integrated Recruitment Technology and CRM Platform Management +2 more programmes
Explore workshops →
Laboratory Specimen Collection and Processing
Train on proper blood draw, sample handling, storage procedures, and chain of custody for lab technicians and phlebotomists.
3+WORKSHOPS
PROGRAMMES
Phlebotomy Techniques for Clinical Trial Protocols Specimen Chain of Custody and Documentation Biospecimen Processing and Aliquoting Standards +2 more programmes
Explore workshops →
Data Management and Statistical Analysis
Learn database design, quality control checks, and statistical methods for data managers and biostatisticians in clinical research.
3+WORKSHOPS
PROGRAMMES
Clinical Data Standards and SDTM Implementation Statistical Analysis Plans for Regulatory Compliance Database Design and Quality Control Procedures +2 more programmes
Explore workshops →
Clinical Research Coordinator Certification
Comprehensive training program covering essential knowledge and skills required for professional clinical research coordinators.
3+WORKSHOPS
PROGRAMMES
Protocol Development and GCP Compliance Management Adverse Event Reporting and Pharmacovigilance Systems Patient Recruitment and Informed Consent Processes +2 more programmes
Explore workshops →
SAS Programming for Clinical Trials
Develop SAS coding skills for data analysis, reporting, and regulatory submissions in clinical trial environments.
3+WORKSHOPS
PROGRAMMES
SDTM and ADaM Dataset Programming in SAS SAS Macro Development for Clinical Data Standardization Advanced PROC SQL for Clinical Trial Analytics +2 more programmes
Explore workshops →
Risk-Based Monitoring and Source Verification
Master modern monitoring strategies, source data verification techniques, and risk management for monitors and auditors.
3+WORKSHOPS
PROGRAMMES
Risk Stratification Models in Clinical Trial Monitoring Source Document Verification and Data Integrity Assessment Central Monitoring Strategy Design and Implementation +2 more programmes
Explore workshops →
Regulatory Submission and NDA Preparation
Train on regulatory documentation requirements, submission formats, and FDA interactions for regulatory specialists and project managers.
3+WORKSHOPS
PROGRAMMES
Module 2.3 Building Comprehensive NDA Dossiers CTD Format Optimization for Regulatory Submissions ICH Guidelines Integration in Submission Strategy +2 more programmes
Explore workshops →