Web Seminars for Clinical Research Professionals
A Barnett Interactive Web Seminar offers you a seamless, secure, multimedia learning experience. These live, instructor-led sessions are designed to be highly interactive, and can be attended by individual attendees or groups at one low cost. No travel, no travel expenses, and no time away from the office!
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FDAEEs Draft Guidance on Integrating Randomized Controlled Trials for Drug and Biological Products into Routine Clinical Practice -
10-Week Establishing a Vendor Qualification and Management Program -
Risk-Based Auditing: Effective Compliance Strategies -
Writing the Clinical Study Protocol -
Strategies for Assessing Risk Tolerance -
12-Hour Statistical Concepts for Non-Statisticians -
Approaches to Address Challenges in Vendor Management -
Data Quality in Clinical Trials: Rationale and Impact -
Subject Recruitment: Proactive Project Plans and Issues Management -
Minimizing Risk in Negotiating Clinical Trial Contracts and Budgets -
12-Hour Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance -
Navigating FDA's June 2024 BIMO Inspection Guidance: A Practical Approach -
Introduction to Statistics for Non-Statisticians -
Electronic Informed Consent Guidance: Regulatory Updates -
RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials -
Key Considerations in Medical Writing: The Clinical Study Protocol, InvestigatorEEs Brochure, Informed Consent Form, and Adverse Events Narratives -
10-Week CRA & CRC Beginner Program -
Good Clinical Practice: Practical Application and Implementation -
Mastering Clinical Research Audits: Effective Responses and CAPA Development -
Writing Pharmacology Sections of an IND Application -
Implementing Quality Agreements -
10-Week Clinical Research Coordinator (CRC) On-Boarding Program -
8-Hour Preparing for FDA Bioresearch Monitoring Program (BIMO) Inspections for Drug Safety -
Identifying Safety Signals in Clinical Trial Data
