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NetZealous LLC DBA GlobalCompliancePanel: 43 products

About GlobalCompliancePanel GlobalCompliancePanel is a training source that delivers diverse, high quality regulatory & compliance trainings. These trainings are simple while being relevant and cost-effective while being convenient. GlobalCompliancePanel imparts knowledge of best practices across a broad range of user-friendly mediums such as webinars, seminars, conferences and tailored, individ…

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21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

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Course "21 CFR Part 11 Compliance for Computer Systems Regulated by FDA" has been pre-approved by RAPS as eligible for up to 12 credits tow…

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GMP requirements for quality control and contract laboratories 2017

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Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products a…

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Regulatory Requirements for Cleaning Validation

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Course "Regulatory Requirements and Principles for Cleaning Validation" has been pre-approved by RAPS as eligible for up to 12 credits towa…

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Validation and Part 11 Compliance of Computer Systems and Data

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Course "Validation and 21 CFR 11 Compliance of Computer Systems: Intermediate to Advanced" has been pre-approved by RAPS as eligible for up…

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Living with Depression – Unveiled Seminar in San Diego

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Course "Living with Depression - Unveiled" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recer…

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Seminar on the Complete Payroll Law 2016

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Overview: This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods a…

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Statistics for the Non-Statistician

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Course "Statistics for the Non-Statistician" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC rec…

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Applied Statistics for FDA Process Validation 2019

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The first stage of process validation is process design. The Process Validation guidance document states, "A successful validation program …

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Best Practice to Set up A Durable Medical Equipment Revenue Program 2016

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Overview: Increased Revenue & Profit For Your Practice! Better Service & Outcomes For Your Patients From Your Existing Patient Base! This s…

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Best Practices for FDA Inspection 2016

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Overview: Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time wi…

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Ensure Your Healthcare Compliance Program 2016

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Overview: The topics will begin with an introduction into the basic healthcare compliance infrastructure necessary to establish a comprehen…

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Promotion and Advertising Practices - FDA Scrutiny 2019

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Description: If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and…

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Validating Radiation Sterilization for Medical Products

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Course "Validating Radiation Sterilization for Medical Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a p…

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Seminar on GMP for Quality Control and Contract Laboratories 2016

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Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products a…

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FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel 2016

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Overview: This seminar will show you how to structure and optimize your QMS. It all starts with Management Responsibility and a commitment …