Live Webinar on : Creating an Effective Contamination Control and Environmental

Monitoring Program Wednesday, June 06, 2012 duration : 01:00 to 02:30 PM EST

Description

Get 15 % Discount as a early bird registrations. Use Promo Key : CGO15

This webinar will enable participants to understand sources of contamination and to investigate various contamination issues in the Biopharmaceutical manufacturing of sterile and non-sterile products. The webinar will also provide an overview of the Environmental Monitoring (EM) program.

Areas Covered in the Session:

Sources of contamination Purpose of Environmental Monitoring Types/frequency of Monitoring Aseptic processing/ Clean Room classifications
Pricing

Environmental data testing and results

Live ( Single registration ) : $189.00 Group ( Max 10 Attendee): $249.00 On Demand (Recording available):$289 Play Back (Unlimited views): $299 Get Training C: $499

Alert/Action limits Controlling contamination

Why should you attend : Contamination issues lead to lengthy investigations and costly recalls. In recent

Who will benefit

Managers, supervisors and general staff working in the following functional areas: Quality Assurance QC Microbiology Laboratory Aseptic Processing areas Cleaning Services Manufacturing Facilities Facility/Process Design Engineering

years there have been a number of FDA actions related to contamination issues. Even the largest pharmaceutical multinationals are not immune, as evidenced by recent recalls of drug products. Creating an effective Contamination Control programs is a key to minimizing these problems and ensuring that your company does not end up as the next TV or newspaper headline. Webinar Includes:

Q/A Session with the Expert to ask your question PDF print only copy of PowerPoint slides 90 Minutes Live Presentation

About Speaker
Henry Urbach is a Management Consultant, Founder and President of GMP TDC LLC, a training, development and consulting company that caters to pharmaceutical and biotechnology industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in Training, QA, and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of remediation , and developing an environmental monitoring training program. He is a dynamic speaker specializing in FDA and ICH compliance, quality systems, and aseptic and environmental monitoring techniques. Henry is a founder and President of GMP Training, Development and Consulting LLC (GMP TDC), a New York-based consulting organization serving Life Sciences industries. He is a Certified Quality Auditor (CQA). His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP Training and Education Association (GMP TEA .

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