All ComplianceOnline clinical Events (14)

Trial Master File (TMF): FDA Expectations from Sponsors and Sites

March 6, 2014 from 10am to 11am – Online Event This training will review the essential elements of a TMF for clinical trials. The activities of set-up, maintenance, and monitoring will be discussed using case studies to highlight common deficienc… Organized by ComplianceOnline | Type: clinical

Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records

February 25, 2014 from 10am to 10am – Online Event This webinar will cover regulatory requirements for archiving clinical trial documents, both paper and electronic records. It will focus on the key components of a digital preservation strategy to en… Organized by ComplianceOnline | Type: clinical
Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover

February 25, 2014 from 10am to 11am – Online Event This 90-minute webinar will help you understand what the true costs are for completing a clinical study and the unanticipated costs that may arise. You will learn about costs that a sponsor must incl… Organized by ComplianceOnline | Type: clinical

Cost-effective auditing: Making the most of the time on-site

February 20, 2014 from 10am to 11am – Online Event This training on clinical audit will teach attendees how to prepare for audit and ensure readiness at all times. Why Should You Attend: How effective are your clinical trial audits? Can you rapidl… Organized by ComplianceOnline | Type: clinical
Cost-effective auditing: Making the most of the time on-site

February 20, 2014 from 10am to 11am – Online Event This training on clinical audit will teach attendees how to prepare for audit and ensure readiness at all times. Why Should You Attend:How effective are your clinical trial audits? Can you rapidly id… Organized by ComplianceOnline | Type: clinical

The European Clinical Trial Directive…Plus…European Filings and Registration Procedures: 2-day In-person Seminar

February 19, 2014 at 8:30am to February 20, 2014 at 4:45pm – Grand Hyatt San Francisco Course Description: This interactive two day seminar will cover the various licensing methods (for Drugs, Biologics & Combination Products) by which applicants can file for product licenses (Mark… Organized by ComplianceOnline | Type: clinical

Best Practices for Clinical Trial Site Selection - Finding High-Enrolling, High-Data Quality Producing Sites

February 13, 2014 from 10am to 11:15am – Online Event This clinical compliance training will provide attendees best practices for clinical trial site selection. Attendees will learn how to identify high-quality and low-quality data sites and how to addr… Organized by ComplianceOnline | Type: clinical
Best Practices for Clinical Trial Site Selection - Finding High-Enrolling, High-Data Quality Producing Sites

February 13, 2014 from 10am to 11:15am Organized by ComplianceOnline | Type: clinical

CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment

December 4, 2013 from 10am to 11:15am – Online Event This Clinical Laboratory Improvement Amendments (CLIA) training will be valuable to CLIA regulated, non-waived laboratories that run automated analyzers or semi-quantitative kit tests. It will highli… Organized by ComplianceOnline | Type: clinical

Foreign Clinical Trials not conducted under an IND (21 CFR 312.120)

September 12, 2013 from 10am to 11:30am – Online Event This webinar will discuss requirements for acceptance of foreign clinical studies, the guidance for foreign investigator qualification, foreign research facility requirements and study monitoring doc… Organized by ComplianceOnline | Type: clinical, webinar