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Clinical Trials Workshops

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Showing 37–48 of 50 categories
Biomarker Analysis and Sample Banking
Train on biomarker collection, storage, analysis workflows, and sample repository management for research scientists.
3+WORKSHOPS
PROGRAMMES
Biospecimen Collection and Chain of Custody Protocols High Throughput Biomarker Assay Development and Validation Sample Banking Infrastructure and Cryopreservation Best Practices +2 more programmes
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Safety Database Management and Reporting
Master safety data systems, adverse event tracking, and periodic safety reports for safety managers and pharmacovigilance specialists.
3+WORKSHOPS
PROGRAMMES
Pharmacovigilance Data Integration and ICSR Standards Real-Time Safety Signal Detection and Statistical Methods Adverse Event Coding Using MedDRA and WHODrug +2 more programmes
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Negotiation and Contract Management
Train on site agreements, budget negotiations, and contract review procedures for project managers and business coordinators.
3+WORKSHOPS
PROGRAMMES
Clinical Trial Agreements: Risk Mitigation and Liability Site Feasibility Agreements and Budget Negotiation Regulatory Compliance in Clinical Trial Contracts +2 more programmes
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Diabetes and Endocrinology Trial Methods
Learn glucose monitoring, metabolic assessments, and disease-specific protocols for endocrinology trial specialists.
3+WORKSHOPS
PROGRAMMES
Continuous Glucose Monitoring Data Integration and Analysis Glycemic Variability Assessment in Endpoint Evaluation HbA1c Standardization and Quality Control Methods +2 more programmes
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Neurology and CNS Study Assessments
Master neurological testing, cognitive assessments, and CNS-specific safety monitoring for neuropsychology professionals.
3+WORKSHOPS
PROGRAMMES
MMSE and MoCA Administration in CNS Trials EEG Monitoring and Artifact Management Protocols Neuropsychological Testing Battery Implementation +2 more programmes
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Regulatory Intelligence and Competitive Tracking
Train on regulatory updates, competitive monitoring, and landscape analysis for regulatory and market intelligence professionals.
3+WORKSHOPS
PROGRAMMES
Regulatory Dossier Intelligence Mining and Analysis Real-time Competitive Landscape Monitoring Frameworks Regulatory Pathway Intelligence for Market Strategy +2 more programmes
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Research Site Licensing and Accreditation
Learn accreditation standards, facility licensing, and quality certifications for site managers and compliance officers.
3+WORKSHOPS
PROGRAMMES
GCP Compliance Auditing for Clinical Research Sites Research Site Capability Assessment and Gap Analysis Regulatory Documentation Management for Site Accreditation +2 more programmes
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Phase 1 Early Stage Study Conduct
Specialize in first-in-human studies, safety escalation, and dose-ranging methodology for early-phase trial coordinators.
3+WORKSHOPS
PROGRAMMES
First-in-Human Dose Escalation Study Design Pharmacokinetic and Pharmacodynamic Sampling Protocols Healthy Volunteer Recruitment and Safety Monitoring +2 more programmes
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Long-Term Safety Surveillance Programs
Master post-approval safety monitoring, registry development, and long-term follow-up protocols for safety specialists.
3+WORKSHOPS
PROGRAMMES
Pharmacovigilance Signal Detection and Management Adverse Event Coding with MedDRA Standardization Risk Evaluation and Mitigation Strategy Development +2 more programmes
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Companion Diagnostics and Test Integration
Train on biomarker-driven trial design, diagnostic test validation, and precision medicine implementations for scientists.
3+WORKSHOPS
PROGRAMMES
Biomarker Qualification and Analytical Validation Workflows NGS Data Integration and Bioinformatics Pipeline Development Assay Development and Clinical Utility Demonstration +2 more programmes
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Compliance Inspections and Warning Letters
Prepare for FDA inspections, manage warning letter responses, and maintain inspection readiness for compliance specialists.
3+WORKSHOPS
PROGRAMMES
FDA 483 Observations Documentation and Response Strategy Warning Letter Root Cause Analysis and Corrective Action Planning Clinical Trial Audit Readiness and Inspection Preparation +2 more programmes
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Statistical Power and Sample Size Calculation
Master power analyses, sample size determination, and statistical design planning for biostatisticians and analysts.
3+WORKSHOPS
PROGRAMMES
Mastering Sample Size Determination for Superiority Trials Non-Inferiority Margin Setting and Power Analysis Adaptive Design Sample Size Reestimation Techniques +2 more programmes
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