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Cyber Attacks, Beyond Disaster Recovery - 2017 from NetZealous001

Tuition: $150.00

Overview: Cyber-attacks and breaches dominate the media and are a significant focus of the government. Businesses and financial institutions are faced with the grim reality that a cyber-attack is...

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Effective Supplier Qualification Program - 2017 from NetZealous001

Tuition: $150.00

Overview: FDA considers the supplier as an extension of your operation. You are liable for supplier’s conduct. FDA will deal with your company in case of product failure, especially as related to...

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Achieving Compliance Excellence - 2017 from NetZealous001

Tuition: $150.00

Overview: We will discuss each of those keys in detail to enhance understanding and to provide the needed information to replicate the approach in your organization. Why should you...

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Validation Program to a Building from Top to Bottom - 2017 from NetZealous001

Tuition: $150.00

Overview: Many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build a sustainable...

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FDA Inspection and Respond to 483 & How to Prepare them - 2017 from NetZealous001

Tuition: $150.00

Overview: In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support...

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CAPA within a Device Quality System - 2017 from NetZealous001

Tuition: $150.00

Overview: You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you. Why should you...

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Environmental Monitoring Program at FDA Regulations - 2017 from NetZealous001

Tuition: $150.00

Overview: Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean...

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Laboratory-Developed Tests - Medical devices 2017 from NetZealous001

Tuition: $150.00

Overview: This presentation will review the legal definition of medical device, and how it is applied by FDA to in vitro diagnostic tests. It will review the history of FDA interest in LDTs, and will...

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ISO 14971 Hazard Analysis at Medical Device - 2017 from NetZealous001

Tuition: $150.00

Overview: The US FDA expects that as part of a product development Design Control Program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a...

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Letters of Credit are issued under the Customs and Practice 2017 from NetZealous001

Tuition: $150.00

Overview: Letters of Credit are the primary instruments for assuring payment of goods sold internationally. Letters of Credit are issued under the Uniform Customs and Practice standard and can be...

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