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Webinars on latest approach to quality objectives

Edited by the Manufacturingtalk editorial team Jan 16, 2007

Free Comprehensive Free Webinars on 21st century approach to attaining Quality Objectives, Statistical Trending and increasing Efficienc

Compliance has become a critical mission for many organisations.

The proliferation of regulations such as Title 21 of the US Code of Federal Regulations Part 11, cGMP, various international guidelines, as well as increased inspection from internal and external auditing agencies have impacted all areas of operations.

Problems associated with laboratory information management, documentation, reporting and personnel training are among those most commonly cited as objectionable during FDA inspections of pharmaceutical manufacturing facilities.

In today's competitive pharmaceutical market, Fortune 500 companies are constantly striving to reach higher levels of process maturity and compliance by adopting high-tech tools.

Novatek's process-based solutions have helped companies meet those objectives.

During these technical webinars, we will present you with a demonstration of Novatek's 21 CFR Part 11 compliant software solutions, the only specialised solutions in the modern pharmaceutical-IT marketplace.

Each webinar will be followed by a 30-minute discussion session featuring a highly respected expert in the field.

The Environmental Monitoring solution webinar will focus on the following areas: * A Process Oriented approach * Quality by Design * Compliance Methodology * Continuous Quality Assurance * Environmental Monitoring data management, control , reporting and trending * Remediation of Risk via Quality Automation * Reducing the total cost of quality translates into increased ROI Moderators: * Dr Frank Kohn, FSK Associates, President * Ms.

Marina Angelozzi, Novatek International, Senior Manager, Technical Sales The Document, Audit and Training Solution webinar will focus on the following areas: * ROI of an automated DATA system * 21 Code of Federal Regulation Part 11 Compliancy * Document and SOP preparation and approval * Assigning and Monitor Trainings and SOPs * Store and access Documents securely * Audit Management via DATA Moderators: * Dr Frank Kohn, FSK Associates, President * Mr Alan Alavi, Novatek International, Senior Manager, Technical Sales The Stability solution webinar will focus on the following areas: * Economic justification for investing in an automated Stability system * Compliance with 21 CFR Part 11 * Data control and reporting * Statistical Analysis of stability data in a paperless system * Intangible benefits Moderators: * Mr Ronald Turton, QCL Quality Compliance Laboratories, Chief Scientific Officer * Mr Sam Torkaman, Novatek International, Associate Director, Sales and Marketing Please note that there is no software to install and no hardware to purchase.