EDM and ERS - Hot Topics and Tools of the Trade

Overview

This 60-minute webinar will address current hot topics impacting EDM and ERS. A high-level overview of the various tools and process’s which are required for the effective and efficient operation of an organizations quality regulated content and document/submission publishing. This holds true whether that is performed by in-house with company resources or through the use of an external service provider. What’s, Whys, Benefits, Risks, etc., will be covered at a high-level.

Continuing Education Credits are not available for this event.

Who should attend?

Professionals involved in:

Regulatory Affairs and Operations
Regulatory Information Management
Global Submission/Project Management
Medical, Technical, and Regulatory Writing
Data Management
Information Technology and Support
Document and eRecords Management
Essential Document Process and Business Systems
Regulatory Standards Implementation
Clinical Operations
Quality Assurance and Compliance
Contract Researchers and Service Support
Emerging Pharmaceutical/Biotech/Device
Vendor Relationship Management

Learning objectives

At the conclusion of this webinar, participants should be able to:

Inform their organization of significant drivers impacting quality regulated content and document/submission publishing
Understand the various processes and best practices associated with quality regulated content management
Understand the various tools associated with document/submission publishing and evaluate those tools against your company’s needs while assuring regulatory compliance

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EDM and ERS - Hot Topics and Tools of the Trade

Overview

Featured topics

Who should attend?

Learning objectives

Be informed and stay engaged.