Bundled Courses

$450.00
3 Webinars To Give Clear Knowledge About OSHA's Fall Protection In General Industry, Mock And OSHA Audit

3 Webinars To Give Clear Knowledge About OSHA's Fall Protection In General Industry, Mock And OSHA Audit

Attending this bundled webinar will give you a clear understanding of your responsibility for Fall Protection, How to prepare and conduct Mock OSHA Audit and toolbox safety talks that don't bore you death.The webinar format is 1-1.5 hours of audio-visual presentation, including a brief Q&A session.This webinar bundle includes below 3 recorded webinars:Fall Protection in General IndustryToolbox Safety Ta..

$600.00
3 Webinars to help you Prepare and Manage an FDA Inspection and Citations

3 Webinars to help you Prepare and Manage an FDA Inspection and Citations

This webinar bundle consists of 3 webinars, which are designed to provide all FDA regulated industries with the information they require to prepare and manage an FDA inspection. The instructors of these webinars will take you through Mock Audits, SOP Inspections, 483 Response Process, and Behaviour during the inspection, several types of 510(K). This bundle will also teach you to prepare a submission to get..

$600.00
4 Best Webinar Courses for Most Effective Recruiting Process

4 Best Webinar Courses for Most Effective Recruiting Process

The bundle of course mentioned below will provide tips and tricks for the effective recruiting process, prescreening, Candidate Sourcing, identify and deliver the best-qualified candidate, ways to review your organization for strengths and areas for growth, ways to increase workforce retention.The webinar format is 1-1.5 hours of audio-visual presentation, including a brief Q&A session.This webinar bund..

$800.00
4 Essential Webinars on FDA's Project Management and Documentation

4 Essential Webinars on FDA's Project Management and Documentation

This bundle of webinars will address approaches to regulatory affairs project management, marketing authorization applications and ongoing management of regulatory obligations. The webinars will also cover batch record review and product release documentation and Breakthrough Therapy Designation, SAE reporting requirements for OTC Drugs, Cosmetics and Dietary Supplements and labeling and recordkeeping regul..

$800.00
4 Valuable Webinars To Understand Computerized System Used In An FDA-Regulated Environment

4 Valuable Webinars To Understand Computerized System Used In An FDA-Regulated Environment

This webinar bundle consists of 4 webinar courses focus on the key aspects of Disaster Recovery and Business Continuity Planning efforts, including best practices and principles for handling this type of work in an FDA-regulated environment, it will also provide guidance on how to keep costs low and avoid “scope creep”, which can lengthen the time and require more money to achieve, learn about FDA oversight..

$600.00
4 Webinar Courses on Complete Policies and Procedures of Form 1-9

4 Webinar Courses on Complete Policies and Procedures of Form 1-9

The bundle of 4 webinars represented below has the complete details about form 1-9 issues that every employer need to know, and how to properly complete the new form 1-9, International work visa’s and how employers handle them. The form I-9 and E-verify to Employment eligibility. The Proper Way to Correct I-9 Documents and Not Pay Penalties.The webinar format is 1-1.5 hours of audio-visual presentation, inc..

$800.00
4 Webinar Courses on FDA Compliance, Clinical Quality Control, Diagnostics, Clinical Data Systems and Computer System Validation

4 Webinar Courses on FDA Compliance, Clinical Quality Control, Diagnostics, Clinical Data Systems and Computer System Validation

This bundle of webinars will help you to understand the steps needed to transfer, validate and maintain an automated assay in the laboratory, heat sterilization is a PROBABILITY function dependent on heat exposure, the number of microorganisms, and the heat resistance of the microorganisms, the TMF includes all of the documentation that a sponsor must record to demonstrate that they have met their obligatio..

$600.00
4 Webinar Courses on Identifying, Reporting, and Preventing the Sexual Harassment

4 Webinar Courses on Identifying, Reporting, and Preventing the Sexual Harassment

The bundle of webinars shown below discuss writing the critical final report of your investigation to minimize harassment liability, drives people to engage in bullying or aggressive behavior at work, What exactly is sexual harassment?, Sexual assault?, Differentiate between flirting and sexual harassment, finding necessary steps to get out of sexual harassment, basics of professional regulatory laws and st..

$1,000.00
5 Effective Webinars To Overcome Life Science Industries Regulatory Challenges

5 Effective Webinars To Overcome Life Science Industries Regulatory Challenges

The objective of this bundled Webinar is to teach participants how to develop their domestic and international strategies for effective reimbursement in parallel to achieving Regulatory Approval, to learn the proper way to set up for a Regulatory Inspection, understand in detail the new requirements for labeling from FDA and EMA, Generation of Controlled Documents and Related Training and will also review t..

$1,000.00
5 Essential Webinars on Documentation, SOP and Labelling Standards

5 Essential Webinars on Documentation, SOP and Labelling Standards

This webinar bundle has webinars addressing the best practices for documentation, FDA, and EMA labeling requirements, generation of controlled documents, investigating deviations, batch record review, and SOP and documenting work instructions.The webinar format is 1-1.5 hours of audio-visual presentation, including a brief Q&A session.This webinar bundle includes below 5 recorded webinars:New FDA and EM..

$1,200.00
6 Webinar Courses on Clinical Quality Control

6 Webinar Courses on Clinical Quality Control

This webinar bundle consists of 6 webinar courses addressing areas like automating assays, applying BTD, sterilization design, QC for analytical materials, new requirements for trial master files, Instrumental liquid chromatography.The webinar format is 1-1.5 hours of audio-visual presentation, including a brief Q&A session.This webinar bundle includes below 6 recorded webinars:Automating Assays for Cli..

$1,050.00
7 Essential Webinars on Cash Flow, Financial Statements and Accounting Fraud

7 Essential Webinars on Cash Flow, Financial Statements and Accounting Fraud

This recorded webinar bundle package contains 7 recorded webinars which cover critical areas like cash flow, forecasting and analyzing cash flow, analyzing financial statements, analyzing the income statement, detect and prevent reimbursement fraud, accounts payable fraud, detecting and preventing employee fraud, TIN compliance, B-Notices, and Audit.The webinar format is 1-1.5 hours of audio-visual presenta..

$1,050.00
7 Essential Webinars on Excel Spreadsheet Productivity Tips for Creating High Impact

7 Essential Webinars on Excel Spreadsheet Productivity Tips for Creating High Impact

This bundle course consists of 7 informative webinars on what you need to know to create an interactive professional-looking dashboard using Excel.The webinar format is 1-1.5 hours of audio-visual presentation, including a brief Q&A session.This webinar bundle includes below 7 recorded webinarsExcel - Creating High Impact Business ReportsCreate a Dashboard with ExcelExcel Spreadsheet Productivity Tips F..

$1,800.00
9 Valuable Webinars on FDA System Requirements and Data Governance for Regulated Industries

9 Valuable Webinars on FDA System Requirements and Data Governance for Regulated Industries

This webinar bundle covers major system and data governance requirements for computer systems regulated by FDA. It also covers systems classification, best practices to prepare for a system validation audit,21 CFR Part 11 compliance, disaster recovery and business continuity planning, mobile applications, planning of functional requirements, testing of systems regulated by FDA, legal regulatory and policy i..

$400.00
A Complete guide for 21 CFR Part 11

A Complete guide for 21 CFR Part 11

FDA’s 21 CFR Part 11 was enacted in the late 1990s and implementation success across the pharmaceutical and other regulated industries have been mixed. There are very specific limitations that arise when using ER/ES capability, such as the elimination of print capability to prevent users from making decisions based on a paper record as opposed to the electronic record. It also requires very specific identif..

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