Nasal decolonization as a tool for infection prevention

This presentation will focus on the risk of MRSA colonization to patients. The current practice of nasal screening and isolation for MRSA colonized patients will be described as well as universal decolonization as an alternative. The products used for decolonization will also be discussed.

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1412&speakerid=251 Compliance Key

Visit: https://www.compliancekey.us/life-science-and-healthcare

Human Error Reduction in GMP Related Environments

Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human errors start at the design stage. From procedures, training, and workplace environment many variables that affect human behavior CAN be manipulated reducing the likelihood of these occurrences. To work with these challenges, it is essential to understand human behavior and the psychology of error as well as understand exactly where the weaknesses of the system are so that they can be improved and/or fixed. This course offers practical approaches and models to address human performance issues in GMP related environments by using a particular methodology to correct, prevent and avoid re-occurrence of these matters

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1402&speakerid=168 Compliance Key

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Federal Labor Standards Act - Wage & Hour Compliance

This webinar will lay the groundwork for determining whether your employees are properly classified as Exempt or Non-Exempt and ensuring that wage and hour laws are being followed properly.

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1382&speakerid=204 Compliance Key

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Background Checks Under the EEOC's Best Practices

This course will cover the use of background checks in the employment process under the EEOC best practices. Being accused of being a discriminatory employer is never a good thing. The cost of having to defend the company against an EEOC accusation can run into the tens of thousands of dollars. Additionally, since EEOC cases are published the poor press and potential loss of business, as a result, makes ensuring you are following the EEOC best practices is important.

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1378&speakerid=92 Compliance Key

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Risk Based Computer System Validation

 FDA requires that all software in computer systems used in GxP activities must be validated. Validation of computer system software is completely different than the validation of device software (embedded software). Validation is much more than testing. It is testing plus design control and configuration management. How to plan and conduct a risk-based validation will be explained. The overall risk for a computer system is a combination of software complexity and product risk as determined by probability, severity and detectability rankings. Also involved in the risk evaluation is the requirement for purchased software supplier qualification. You'll learn how to integrate risk-based supplier evaluation into the validation process. Validation Master plan and System Validation Plans will be explained Testing, based on risk, includes requirements validation and IQ, OQ and PQ. A procedure for each level of complexity and risk will be described.

Register: https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1418&speakerid=48

Compliance Key

Visit: https://www.compliancekey.us/life-science-and-healthcare