Setting Up and Running a Tougher Supplier Audit Program

Compliance4All announces webinar on the topic, “Setting Up and Running a Tougher Supplier Audit Program” on October 21. This webinar will discuss and evaluate the nature of change a company has to bring about in meeting FDA expectations for a supplier audit program.

Fremont, CA: Compliance4All, a provider of cost-effective regulatory compliance trainings for a wide range of regulated industries, will organize a webinar on the topic, “Setting Up and Running a Tougher Supplier Audit Program” on October 21. John E. Lincoln, a senior medical device and regulatory affairs consultant, will be the Speaker at this session.

About the webinar:

The FDA is working hard to change the perception among the public perception that it has been ineffective in protecting the public. In order to dispel this belief; it is working harder than perhaps ever before to become more stringent in its function of being a strict regulatory body.

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

Most Warning Letters will not have an initial judicial review, resulting in more and faster Warning Letter filings. Larger, higher profile companies are coming under FDA investigation activities. Companies are outsourcing more; with some thinking they can outsource some of their cGMP compliance as well. In line with this thinking, the FDA has indicated that a key area gaining attention is a company’s suppliers, for services and products/components.

This change in attitude on the part of the FDA requires major changes in the way the industry thinks and adapts to the FDA’s line of thinking. It must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. This webinar will discuss and evaluate the nature of change a company has to bring about. The speaker will explain industry’s selection, audit, use and on-going relations with its suppliers of services and products/components.

About the Speaker:

John E. Lincoln is a Medical Device and Regulatory Affairs consultant.

John E. Lincoln, a graduate of UCLA, is a medical device and Regulatory Affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management and U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and have been described in peer-reviewed technical articles and workshops worldwide.

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/