Browse 452 health, safety & security courses in USA
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Clinical Trial Applications in China Latest 2018
provided by
Compliance4All
Overview: China FDA (CFDA), now renamed as CNDA, made a series of significant changes to the clinical trial regulations, issuing a large number of guidelines and opinions in Chinese. As an important ...
Overview: China FDA (CFDA), now renamed as CNDA, made a series of significant changes to the clinical trial regulations, issuing a large number of guidelines and opinions in Chinese. As an important ...
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Risk Control According to (GxP-GMP) Requirements
provided by
Compliance4All
Overview: GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. Documentation is a critical tool for ensuring ...
Overview: GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. Documentation is a critical tool for ensuring ...
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Highlights of FDA GLP Regulations and the (Roles) and Responsibilities
provided by
Compliance4All
Overview: This 3 hour GLP virtual seminar will discuss various GLP regulations (FDA/OECD GLP's) along with highlighting roles and responsibilities of management and key personnel involved in drug development, ...
Overview: This 3 hour GLP virtual seminar will discuss various GLP regulations (FDA/OECD GLP's) along with highlighting roles and responsibilities of management and key personnel involved in drug development, ...
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FDA During New (Drug) Development 2018
provided by
Compliance4All
Overview: Why is it important to engage with the FDA? To discuss your development plan to support NDA or BLA regulatory submission To identify and mitigate potential issues early To identify any critical ...
Overview: Why is it important to engage with the FDA? To discuss your development plan to support NDA or BLA regulatory submission To identify and mitigate potential issues early To identify any critical ...
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Advanced PowerPoint Tips and Tricks 2018
provided by
Compliance4All
Overview: This webinar will show you the basics of getting started with PowerPoint, and how to start to build impactful presentations. You will learn how to build a presentation from scratch, how to easily ...
Overview: This webinar will show you the basics of getting started with PowerPoint, and how to start to build impactful presentations. You will learn how to build a presentation from scratch, how to easily ...
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Assessing and Planning for Risk (Latest 2018)
provided by
Compliance4All
Overview: Project risk is greater the longer your project lasts, the longer the time between preparing your project plan and starting the work, the less experience you, your team members, or your organization ...
Overview: Project risk is greater the longer your project lasts, the longer the time between preparing your project plan and starting the work, the less experience you, your team members, or your organization ...
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Controlling Human Error in the Manufacturing Floor (New 2018)
provided by
Compliance4All
Overview: This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence ...
Overview: This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence ...
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FDA continues to enforce through its new 21 CFR Part 11 inspection
provided by
Compliance4All
Overview: The webinar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their ...
Overview: The webinar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their ...
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cGMPs in the Quality Control Laboratory (Medical 2018)
provided by
Compliance4All
Overview: In this webinar we will apply one aspect of this proactive approach, the review regulatory requirements and analysis of 483 and Warning Letter observations to determine if similar observations ...
Overview: In this webinar we will apply one aspect of this proactive approach, the review regulatory requirements and analysis of 483 and Warning Letter observations to determine if similar observations ...
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Quality Agreements Made Easy (Advanced 2018)
provided by
Compliance4All
Overview: The requirements for the assurance of quality within networks and circles of entities whose responsibilities are increasing specialized present an especially vexing challenge to the managements ...
Overview: The requirements for the assurance of quality within networks and circles of entities whose responsibilities are increasing specialized present an especially vexing challenge to the managements ...
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