Webinar on Building a Compliant Documentation and Training System

Website https://compliancetrainings.com/product/building-a-compliant-documentation-and-training-system-3/ | Edit Freely

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

Deadline: January 27, 2017 | Date: January 27, 2017

Venue/Country: Online, Canada

Updated: 2016-12-19 22:34:41 (GMT+9)

Call For Papers - CFP

There is an increasing trend for regulatory agencies to view compliance documentation and training with increased scrutiny. Documentation and training that is improperly developed, implemented, and/or recorded presents a significant regulatory risk for manufacturers. In addition to meeting regulatory requirements, documentation and training, that is properly developed, also can serve as the basis for a well-controlled operation and a highly-competent workforce.

Areas Covered in the Session :

Global regulatory requirements for compliance documentation and training

The relationship between compliance documentation and training

Read and understand versus demonstrated competence

Regulatory requirements

Elements of a compliant documentation and training system

How to conduct a compliance documentation and training analysis

Compliance documentation and training as the basis for world-class operational control and performance improvement

Who Will Benefit:

A must attend webinar for all personnel / companies in the Pharmaceuticals, Medical Devices, Biotechnology, Cosmetics, Personal Products, Foods & Beverages fields. The professionals who will benefit include all:

Training Managers and Directors

Regulatory Affairs

Quality Professionals

Documentation department

Compliance officer

Product Development Professionals

QA/QC analysts

Internal Auditors

Quality Assurance scientists

Production

Operations

Consultants

Quality Unit managers and supervisors