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Paid Sick and Family Leave: Multi-State Updates for Mastering Emerging Compliance Obligations
Janette Levey Frisch
90 Min
Product Id: 705659
In this paid sick leave and family leave webinar, learn the upcoming updates related to – legal PTO policy, carryover and notice/posting requirements, PTO leave with protected leave under FMLA, PTO accrual rates, PTO and the exempt employee, pregnancy disability leave, caps on vacation banks.
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How to Take Advantage of Letters of Credit for Importers-Exporters
Douglas Cohen
60 Min
Product Id: 706196
In recognition of the challenges associated with the execution of international payment terms, this webinar will provide both importers and exporters with the insight necessary to make well-informed credit decisions. The webinar uses a combination of easy-to-understand explanations and real-life scenarios, ideal to credit managers, international salespeople, logisticians and order management personnel.
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6-HR Virtual Seminar - SOP's and Work Instructions, Training, and Compliance in the Life Sciences
Charles H Paul
6 Hrs
Product Id: 706182
This seminar will explore the unique and critical relationship between regulatory compliance, compliance documentation, and technical operations training and improved performance, standardization and world class regulatory compliance. We will also discuss the area of training in regulated environments, its importance, and its relationship to compliance documentation.
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What Employers Need to Know about Legalized Marijuana
Rebecca Jacobs
60 Min
Product Id: 706180
This webinar will discuss employers’ rights and obligations with respect to employees’ use of legalized marijuana for medicinal or recreational use. With a number of states legalizing either or both type of use, employers must keep on top of the current trends, especially in light of the fact that marijuana is still a controlled substance under federal law.
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Regulatory Inspections - How to prepare for a visit from an FDA Auditor
Joy McElroy
60 Min
Product Id: 705725
This FDA audit webinar will highlight the purpose of FDA audits and scope, Understanding of QSIT audit and how to develop an audit preparedness plan. It will also give understanding of what the FDA will look for at the conclusion of your audit and how to communicate with FDA before and after the audit.
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Understanding FDAs Governance of Prescription Drug Development: Manufacturing/cGMPs, Submission Process and Post Approval Commitments - Part 2
Sharon W Ayd
60 Min
Product Id: 706159
In this webinar, we will review in detail major considerations to be well-thought-out during the prescription drug product development process. We will review in depth FDA cGMPs and their importance in drug manufacturing. We will review the submission process and post-approval commitments. This webinar is Part 2 of a 2 Part series.
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The Regulation of in-house IVDs and accreditation of laboratory users in Australia
Paul Cohen
75 Min
Product Id: 706155
Attend this webinar to understand the definitions of in-house IVDs, the regulatory requirements including classification & essential principles, the NATA requirements related to how and when IVDs can be used as a research or diagnostic tool and the current laboratory supervision requirements for the ability to perform and report on in house IVDs.
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How to Create an Effective GMP Compliant Training Program and Reduce Training Related Human Errors
Ginette M Collazo
90 Min
Product Id: 706179
Attend this webinar to learn how to create a GMP compliant training program and avoid human errors when implementing/improving a training program. It will discuss important elements like curricula, training management systems, training effectiveness and more.
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Is Your Compliance Program Due for an Update?
Jim Kandler
60 Min
Product Id: 705085
This training program will highlight common issues that occur over time with material compliance programs, and demonstrate how to address them. This can result in a more effective and responsive material compliance effort for your company.
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Achieving Sustainability Results with ISO 26000
Kelly Eisenhardt
60 Min
Product Id: 705079
The International Standards Organization (ISO) defined the ISO 26000 guideline for the use and planning of all structured, measured, and monitored social responsibility programming. This standard enables companies to initiate and track performance of CSR programs by focusing on the triple bottom line (TBL) - people, planet, and profit. This training program will offer in depth look at the key components of the ISO 26000 guideline and best practices to implement and support a social responsibility program.
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Understanding the ISF 10+2, 10+5 And Its Processes
Charles Jacque
60 Min
Product Id: 706195
The webinar covers the need for understanding the ISF 10+2, 10+5 and its processes. The reason for filing the ISF, when to file the ISF and who files the ISF.
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Understanding FDAs Governance of Prescription Drug Development: Interacting with FDA, Established Pathways to Approval, cGMP and Clinical Study Concerns – Part 1
Sharon W Ayd
90 Min
Product Id: 706130
This webinar will review in depth FDA and other important US Regulatory Bodies roles and responsibilities pertaining to the prescription drug development process. We will explore the recognized regulatory approval pathways, good clinical practice and clinical study concerns.
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Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Carl Patterson
60 Min
Product Id: 706177
In this webinar, get an overview of auditing for microbiological aspects of pharmaceutical and biopharmaceutical manufacturing. It will cover pertaining regulations and their applications to provide success when being reviewed by an auditor.
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The Big Data Health in the Brazilian Regulatory Affairs
Eliana Silva de Moraes
90 Min
Product Id: 706173
Attend this webinar to get an overview of the recent Brazilian changes regarding the big data protection in Regulatory Affairs. It is an opportunity to analyze and discuss key issues related to the data protection applicable to all medical, pharmaceutical, food and cosmetic product.
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Essentials of IT Auditing for the Non-IT Auditor
Robert Davis
60 Min
Product Id: 706172
Information Technology (IT) is a critical enabler of business. Assuring an enterprise's governance, including risk management and control processes, requires auditors to understand the role of IT within their organizations and to develop adequate knowledge and skills to audit IT systems as the line separating "IT" and "non-IT" audits are beginning to disappear, except in the very technical IT domains. This course is designed to give non-IT auditors and beginning information security professionals an overview of the various considerations and aides in audit planning to gain a greater understanding of how to evaluate defined audit areas.
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Supplemental Pay Essentials - Severance Pay, Deferred Compensation, Recordkeeping and Fringe Benefits
Patrick A Haggerty
90 Min
Product Id: 704112
This training program will help attendees distinguish between supplemental wage payments and regular wage payments and help them identify wage payments that are neither supplemental nor regular. It will also detail methods used to compute withholding on supplemental pay including examples.
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Backup Communications for Medical Facilities - New Federal Regulations Affect Healthcare Providers and Amateur Radio
Michael Abitz
60 Min
Product Id: 706171
Amateur Radio’s primary purpose for existing is to provide backup communications in times of disaster. The webinar presents methods used to provide communications when Internet and Phone Systems are not accessible due to human-made or natural disasters.
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Detecting and Preventing Fraud in Payroll: Proven Strategies to Save Money
Peter Goldmann
90 Min
Product Id: 706025
Attend this highly informative 90-minute webinar to find out the different kinds of payroll scams, how to identify red-flags of fraud and how to prevent and stop payroll fraud.
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Changing Payroll Frequencies: How It Can Be Done 2019
Vicki M. Lambert
90 Min
Product Id: 704483
This webinar will allow attendees to gain the knowledge and insight necessary to successfully implement changes of payroll frequency for your company.
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How to Comply with the Chemical Facility Anti-Terrorism Standards (CFATS)
Joe Keenan
60 Min
Product Id: 706187
Attend this webinar to understand the Chemical Facility Anti-Terrorism Standards (CFATS) in detail. Site-specific Chemical Facility Anti-Terrorism Standards (CFATS) questions and answers, as well as potential scenarios, will be addressed.