Recorded Webinars


Preventing Human Error in the Life Sciences - Pharmaceutical and Medical Device

Preventing Human Error in the Life Sciences - Pharmaceutical and Medical Device

Overview: Human Error occurs in all settings.  In the world of pharmaceutical and medica..

Date : 29th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Error Resolution - Regulation E vs ACH Rules - What to Know?

Error Resolution - Regulation E vs ACH Rules - What to Know?

Overview: In this 90-minute session, Returning Unauthorized transactions using Reg E or the N..

Date : 28th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Functional and System Requirements for Systems Regulated by FDA

Functional and System Requirements for Systems Regulated by FDA

Overview:Computer System Validation (CSV) has been regulated by FDA for more than 35 years, as it re..

Date : 27th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 1 Hour 40 Mins

Form I-9 Compliance Flexibility Rules - New Deadline and Things to Keep in Mind

Form I-9 Compliance Flexibility Rules - New Deadline and Things to Keep in Mind

Overview: The COVID-19 Pandemic has changed the way all of us do business.  As a resu..

Date : 20th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

The 6 Most Common Problems in FDA Software Validation and Verification - What to Know?

The 6 Most Common Problems in FDA Software Validation and Verification - What to Know?

Overview:This webinar describes the validation planning process with particular emphasis on avoidin..

Date : 14th July 2022

Time : This Event is Over

Duration : 90 Mins

An Advanced Course on Lean Documents, Lean Configuration, and Document Control

An Advanced Course on Lean Documents, Lean Configuration, and Document Control

Overview:Just as a manufacturing process produces a product, controlled documents are the product o..

Date : 13th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 1 Hour 30 Mins

Complying with Employment Record Requirements in 2022 - Checklist

Complying with Employment Record Requirements in 2022 - Checklist

Overview: The failure to maintain adequate and sufficient time keeping records under the Fair L..

Date : 30th June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Writing Effective SOPs for the Medical Device and Pharmaceutical

Writing Effective SOPs for the Medical Device and Pharmaceutical

Overview: Standard Operating Procedures (SOPs) are a critical ingredient in an effective and ef..

Date : 30th June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Preventing Medical Device Recalls – A Prevention Strategy

Preventing Medical Device Recalls – A Prevention Strategy

Overview:  In a recent study, the FDA has reported a 95% increase in medical device recalls ..

Date : 28th June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Mandatory Paid Sick Leave vs Vacation vs PTO: What to Know?

Mandatory Paid Sick Leave vs Vacation vs PTO: What to Know?

Overview: Fifteen states and the District of Columbia now require employers to provide paid sic..

Date : 24th June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Best Practices in Preparation for an FDA Computer System Audit

Best Practices in Preparation for an FDA Computer System Audit

Overview: FDA requires that all computer systems used to produce, manage and report on “GxP” (G..

Date : 23rd June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Excel Spreadsheets - Data Integrity and 21 CFR Part 11 Compliance

Excel Spreadsheets - Data Integrity and 21 CFR Part 11 Compliance

Overview: This interactive webinar explains how to configure and validate a GxP compliant sprea..

Date : 23rd June 2022

Time : This Event is Over

Duration : 90 Mins

FDA Technology Modernization Action Plan and Impact on Regulated Computer Systems

FDA Technology Modernization Action Plan and Impact on Regulated Computer Systems

Overview: Computer system validation has been regulated by FDA for more than 30 years, as it re..

Date : 31st May 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 1 Hour 30 Mins

Form I-9 Compliance Flexibility Rules - New Deadline and Things to Keep in Mind

Form I-9 Compliance Flexibility Rules - New Deadline and Things to Keep in Mind

Overview: The COVID-19 Pandemic has changed the way all of us do business.   As a r..

Date : 27th May 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 01 Hour 35 Mins

NEW Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities

NEW Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities

Overview:Recent updates to the Nacha Operating Rules are further clarifying the Roles and Responsibi..

Date : 26th May 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 01 Hour 30 Mins

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