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Clinical Compliance - Documentation & Proceedings

> Conference documentation, webinars & Proceedings

Recommended
Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment

This 90-minute webinar on Disinfection and Cleanroom Cleaning will cover effective ways to rotate disinfectants, most current industry methods for applying disinfectants and effective methods for controlling residues.

By : Compliance Online
Product Type : On Demand Webinar
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

This clinical trial audit webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit.

By : Compliance Online
Product Type : On Demand Webinar
Trial Master File for Research Sites: Can You Pass FDA Inspection?

This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.

By : Compliance Online
Product Type : On Demand Webinar
Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe

Understand what is the CER and how to prepare for and defend it and properly constructing a "bullet-proof Technical File and manage your documentation.

By : Compliance Online
Product Type : On Demand Webinar
Clinical Statistics for Non-Statisticians. An Introduction to Statistical Concepts and Practices-Webinar

In this Clinical Statistics webinar/training all topics will be taught from a practical, non-theoretical perspective for non-statisticians & value and meaning of descriptive statistics including the use of normal vs. non-normal statistics.

By : Compliance Online
Product Type : On Demand Webinar
Fundamentals of FDA’s Clinical Trial Audits – A Must- Know for Audit preparation

This Clinical Trial Audits webinar will provide help both CRAs and sites utilize quality improvement methods and effectively prepare for upcoming GCP audits.

By : Compliance Online
Product Type : On Demand Webinar
3-hr Virtual Seminar - China: Compliance Processes for Life Science Products

This 3-hr virtual seminar on compliance processes for life science products in China will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.

By : Compliance Online
Product Type : On Demand Webinar
Auditing Systems for 21 CFR Part 11 Compliance - Webinar By ComplianceOnline

This webinar will present a methodology for system assessment, risk-analysis, 21CFR Part 11 compliance, remediation and inventory, along with templates and forms that attendees can modify for their own business.

By : Compliance Online
Product Type : On Demand Webinar
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar

This training will address the regulatory requirements which apply at the various stages of development, and suggest proven strategies for compliant and phase-appropriate analytical method validation.

By : Compliance Online
Product Type : On Demand Webinar
Environmental Monitoring and Contamination Control Plan - Webinar

This 90-minute cleanroom contamination control training will review the common mistakes that people make in cleanrooms that lead to contamination, show how to develop a successful contamination control program and discuss ways to improve your facility's design and maintenance.

By : Compliance Online
Product Type : On Demand Webinar
OSHA Recordkeeping: Recent Recordkeeping Interpretations

This OSHA Recordkeeping training class will incorporate the lessons learned from OSHA’s recent Interpretation Letters into the existing OSHA recordkeeping analysis as well as OSHA’s current Frequently Asked Questions.

By : Compliance Online
Product Type : On Demand Webinar
The Odds are Against Auditing: Statistical Sampling in Audit

This webinar will cover different statistical sampling strategies and the risk management strategies while auditing.

By : Compliance Online
Product Type : On Demand Webinar
FDA's 2011 Draft Guidance on Financial Disclosure by Clinical Investigators

This webinar will help you understand FDA’s draft guidance on financial disclosure by clinical investigators and show how financial information should be disclosed to FDA.

By : Compliance Online
Product Type : On Demand Webinar
Bioanalytical Methods Validation - Webinar

Best practices of Bioanalytical method validation, including components of a validation, how to include critical reagents comparison, selectivity experiments, assessment of stability. Concept of plate and experiment separation.

By : Compliance Online
Product Type : On Demand Webinar
How to secure GCP compliance in Clinical Trials

This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense.

By : Compliance Online
Product Type : On Demand Webinar