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Clinical Trials Workshops

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Showing 13–24 of 50 categories
Biostatistics and Study Analysis Fundamentals
Build foundational statistical knowledge for clinical trial design, analysis, and interpretation for researchers and analysts.
3+WORKSHOPS
PROGRAMMES
Statistical Analysis Plan Development and Implementation Efficacy and Safety Data Analysis Methods Pharmacokinetic and Pharmacodynamic Modeling Fundamentals +2 more programmes
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Quality Assurance and Audit Procedures
Learn audit techniques, quality inspections, and compliance verification for QA specialists and internal auditors.
3+WORKSHOPS
PROGRAMMES
GCP Compliance Auditing in Clinical Trial Operations Quality Risk Management Framework Implementation Data Integrity and ALCOA Principles Verification +2 more programmes
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Pharmacokinetics and Pharmacodynamics Basics
Understand drug absorption, distribution, metabolism concepts for clinical research and medical science professionals.
3+WORKSHOPS
PROGRAMMES
Compartmental Modeling and PK Parameter Estimation Bioavailability Assessment and Bioequivalence Studies Dose Response Relationships and PD Modeling +2 more programmes
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CTMS Software Implementation and Management
Master Clinical Trial Management Systems configuration, data workflows, and reporting capabilities for administrators and coordinators.
3+WORKSHOPS
PROGRAMMES
CTMS Database Configuration and Custom Field Mapping Clinical Trial Master Scheduling and Resource Allocation CTMS Data Integration and Third Party System Interfaces +2 more programmes
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Patient Safety Assessment and Monitoring
Train on vital signs, laboratory values, and safety assessment protocols for clinical staff and monitoring specialists.
3+WORKSHOPS
PROGRAMMES
Adverse Event Coding and MedDRA Classification Mastery Safety Data Mining and Signal Detection Methods Serious Adverse Event Assessment and Reporting +2 more programmes
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Medical Coding and Diagnosis Classification
Learn ICD-10, MedDRA coding, and medical terminology for data entry and coding professionals in clinical research.
3+WORKSHOPS
PROGRAMMES
ICD-10-CM Coding for Clinical Trial Adverse Events MedDRA Coding Standardization in Drug Safety Assessments SNOMED CT Implementation for Clinical Trial Data Harmonization +2 more programmes
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Investigator Site Initiation and Setup
Train on site setup procedures, investigator meetings, and pre-study activities for site managers and startup coordinators.
3+WORKSHOPS
PROGRAMMES
Protocol Assessment and Site Feasibility Evaluation Regulatory Documentation Preparation for Trial Initiation Site Activation Workflows and CTMS Implementation +2 more programmes
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eSource and Real-World Evidence Collection
Master electronic source documentation, patient-reported outcomes, and real-world data integration for modern trial coordinators.
3+WORKSHOPS
PROGRAMMES
Electronic Health Record Integration for Clinical Trials Real-World Data Capture Using Digital Patient Engagement Platforms eSource Data Quality Assessment and Audit Readiness +2 more programmes
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Blinding and Randomization Techniques
Learn study masking procedures, randomization processes, and data stratification for study coordinators and data managers.
3+WORKSHOPS
PROGRAMMES
Implementing Double-Blind Study Designs Effectively Stratified Randomization and Block Randomization Methods Interactive Response Technology for Centralized Randomization +2 more programmes
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Microbiology and Virology Testing Methods
Train on laboratory testing procedures, pathogen identification, and quality control for lab technicians in infectious disease trials.
3+WORKSHOPS
PROGRAMMES
Viral Isolation and Culture Techniques in Clinical Trials Real-Time PCR and qPCR Assay Development for Virology Microbial Identification and Characterization Using MALDI-TOF +2 more programmes
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Immunogenicity Assessment and Bioanalysis
Develop expertise in immune response measurement, antibody testing, and bioanalytical methods for laboratory professionals.
3+WORKSHOPS
PROGRAMMES
LC-MS/MS Method Development for Immunogenicity Biomarkers ADA Detection and Neutralizing Antibody Characterization Flow Cytometry Assay Design for Immune Response Profiling +2 more programmes
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Clinical Research Ethics and IRB Process
Master institutional review procedures, ethical principles, and IRB submission requirements for researchers and ethics board members.
3+WORKSHOPS
PROGRAMMES
Protocol Submission and IRB Review Navigation Informed Consent Form Development and Optimization Risk Benefit Assessment for Clinical Trial Ethics +2 more programmes
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