21st Century Validation

Compliance4All announces webinar on the topic, “21^st Century Validation” on October 30. This webinar will offer insights into the evolving concepts that help validation meet regulatory expectations.

Fremont, CA: Compliance4All, a provider of cost-effective regulatory compliance trainings for a wide range of regulated industries, will organize a webinar on October 30. The topic of this webinar is “21^st Century Validation”, and the speaker is Sam DeMarco, President of Compliance Team, Inc.

About the webinar:

Many pharmaceutical manufacturing companies are still finding meeting global regulatory compliance expectations right quite a challenge. Over the past couple of decades or so, FDA and EU regulatory expectations have evolved considerably, as a result of which a new ‘improved’ validation approach that offers validation and engineering organizations the possibility of streamlining and simplifying validation activities is emerging.

For more information or to register for the webinar, please click here.

This new approach will help organizations control costs associated with building and starting new facilities and engineered systems. It also holds the promise of enabling organizations to channelize their limited technical resources optimally, making them spend less time and energy for working on gaining better process knowledge needed for optimizing process capability.

The speaker at this webinar will talk at length on this approach. In addition, he will discuss the “why” and “what” and the events and background that have impacted validation over the last 25 years.

He will emphasize the importance of an organization’s Quality System for validation. This will help attendees identify existing and potential gaps in their validation programs. The webinar will discuss the importance of focusing on critical aspects and having meaningful, well-written User Requirements Specifications as key elements of establishing a streamlined and simplified validation program for capital projects.

About the Speaker:

Sam DeMarco is a senior compliance consultant and president of Compliance Team, Inc. Sam has over 25 years of technical, managerial, and consultative experience in the pharmaceutical and medical device industries.

His subject matter expertise covers a broad area of knowledge, which includes engineering, commissioning, validation, project management, quality assurance, and pharmaceutical manufacturing and product quality compliance.

About Compliance4All:

Compliance4All (http://www.Compliance4All.com/) is a specialized offering from NetZealous, a Fremont, CA-registered organization. It is a source for a wide range of professional trainings, compliance trainings and consulting for the regulated industries. Compliance4All offers a broad range of high quality, affordable regulatory and compliance-related services relating to medical devices, pharmaceutical, FDA, clinical trials, laboratory compliance, biologicals, drugs, food and biotechnology.

Many professionals in the various areas in which Compliance4All offers its trainings have benefited from the vast experience of its well-known speakers, who are reputed globally in their respective fields.

Contact information:

Call: 1-800-447-9407;

Visit: http://www.netzealous.com/