Webinar on Effective Standard Operating Procedure (SOPs) Development for Regulatory Compliance

Website https://compliancetrainings.com/product/effective-standard-operating-procedure-sops-development-for- | Edit Freely

Category Clinical & Laboratory, FDA Compliance, Food, Drugs & Biologics, Medical Devices

Deadline: January 10, 2017 | Date: January 10, 2017

Venue/Country: Canada, Canada

Updated: 2016-12-02 21:12:49 (GMT+9)

Call For Papers - CFP

Learn how to meet their expectations and fulfill their requirements, so your documents are approved quickly, and there are no complications or problems. For preparing the documents, you need to know how to format SOPs, what elements to include in them, and how to write effective and efficient documents. You also need to know the roles and responsibilities of SOP authors and reviewers, and how to define roles in SOPs.

Areas Covered in the Session :

SOPs and their relation to the regulations

Why written procedures are beneficial

FDA expectations for written documents and Regulatory Requirements

Developing an effective review and approval process compliant with regulatory requirements

How to implement a training program for document creation and review

A system for the control, archival, and disposal of written procedures

Formatting SOPs

Elements to include other than the procedure

How to write effective but efficient documents

Roles and responsibilities of authors and reviewers of SOPs

How to define roles in SOPs for supervisors and operators

Who Will Benefit:

Quality Managers

Quality Engineers

Production Teams

Research and Development Teams

Compliance Teams

Documentation Teams

GxP

Regulatory Affairs Teams

Consultants

Small Business Owners