Information Technology
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2 Hours Virtual Seminar on Practical Excel Techniques for Lookup Functions
Are your spreadsheets lacking the integrity and resilience you wished for? This webinar presented by Excel expert David Ringstrom, CPA, will prove to be extremely insightful and helpful. We will take a deep dive into a variety of worksheet... -
2-Hour Virtual Seminar on Excel as a BI Tool – Power Pivot and Power Query 101
Power Pivot and Power Query are free addins for Excel, written by Microsoft (in fact in Excel 2016 and later Power Query is built into the application and not an addin at all). Power Pivot puts the “power” into... -
2-Hour Virtual Seminar on Practical Excel Pivot Tables
In this empowering and insightful presentation, Excel expert David Ringstrom, CPA, teaches you the basics of creating and using Excel pivot tables. He will then take you beyond pivot table basics and shows you step-by-step how to manipulate pivot... -
2-Hour Virtual Seminar on Practical Excel Techniques for Payroll Professionals
Payroll professionals might not be aware of the many features and functions available in Excel that can be used to improve the accuracy and efficiency of their payroll production. In this valuable webinar, Excel expert David Ringstrom, CPA, demonstrates... -
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21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
This seminar will help you understand in detail the application of FDA’s 21 CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation... -
21 CFR Part 11 Compliance for Electronic Records and Signatures
Companies want to transition to electronic records but are afraid of compromising their quality system and receiving 483’s at their next inspection. Part of this fear originates from confusion. FDA originally published a rather severe 21 CFR Part 11.... -
3 hour Virtual Seminar on HIPAA – How to Put a Comprehensive Compliance Program in Place
Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited... -
3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it... -
3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out
Standard Operating Procedures (SOPs) are necessary to demonstrate compliance with regulations and operational practices. It also serves as a documented roadmap which ensures consistency. This is integral to a strong quality system. If you want to improve SOPs writing... -
3-Hour Virtual Seminar on Excel Spreadsheet Validation for FDA 21 CFR Part 11
Spreadsheets such as Excel, are available for creating a wide range of end user applications, including widespread use in the laboratory, creating customized statistical analyses, the creation of local databases, data mining, and multivariate analysis. These may be used... -
3-Hour Virtual Seminar on IEC 62304 and Demystifying Software Validation using the Principles of LDLC
If your company need to file for 510K approval for Software as a Medical Device (SaMD) or software enabled medical Devices to the FDA for, this webinar is for you. After waiting for seven or more months to find... -
3-Hour Virtual Seminar on Project Management for Computer Systems Validation
Project Management is defined as the planning and organization of an organization’s resources in order to move a specific task, event or duty toward completion. However, Validation of Computerized Systems has a very specific set of tasks that are... -
3-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance
This seminar will focus on cybersecurity of medical devices, a key concern for those who develop, manufacture, test, and distribute these products. Protecting medical devices from hacking where someone can alter the actual code embedded in the device could... -
4-Hour Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
Electronic record/electronic signature (ER/ES) capabilities are extremely important and should be built into FDA-regulated computer systems to meets compliance with 21 CFR Part 11. This webinar will help you to strategize the development of a company philosophy and approach,... -
4-Hour Virtual Seminar on Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Computer systems used in conducting clinical trials must be evaluated to determine the level of compliance, established on validation and data integrity. We will walk through the entire System Development Life Cycle (SDLC) approach to validation of FDA-regulated computer... -
4-Hour Virtual Seminar on Quality Control Laboratory Compliance – cGMPs and GLPs
FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries – pharmaceuticals, biologics, medical devices, as well as foods and cosmetics – as...