IT Change Management

Know everything about 21 CFR Part 11 compliance and how to control electronic signatures and electronic records. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/21-CFR-Part-11-Electronic-Record-and-Signature-Validation-508215/JULY-2018-ES-TRAININGREGISTRY

This webinar provides initial guidance on how to build a cybersecurity recovery program that includes FDA CAPA elements. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Cybersecurity-Exploitation-Recovery-503341/MAY-2018-ES-TRAININGREGISTRY

The purpose of this webinar is to train technical writers in general guidelines for the creation and maintenance of documents. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Technical-Writer-Training-509352/MAY-2018-ES-TRAININGREGISTRY

This training on FDA software validation related warning letters will discuss what to do to avoid additional software related compliance issues along with the response steps where the citations directly or indirectly include automated system. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/FDA-Warning-Letter-Consent-Decree-Software-Validation-505191/FEBRUARY-2018-ES-TRAININGREGISTRY

Many companies struggle with spreadsheet compliance. Some are still using invalidated spreadsheets. Many companies lack an understanding of how to satisfy FDA technical validation requirements as applied to spreadsheets. Most organizations lack a clear spreadsheet compliance strategy. An unplanned 'emergency' spreadsheet validation project could paralyze the organization. This webinar will describe methods for planning and executing spreadsheet validations that satisfy FDA requirements. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Spreadsheet-Validation-Understanding-and-Satisfying-FDA-Requirements-504170/JANUARY-2018-ES-TRAININGREGISTRY

This webinar is designed to provide both a regulatory compliant and practical overview of Good Laboratory Practice (GLP) requirements (21 CFR 58). GLP is both critical in meeting current regulatory requirements, and in ensuring efficient and cost-saving quality laboratory operations.GLP regulations span general provisions, organization and personnel, facilities to records and reports. FDA regulatory compliance requirements will be reviewed, along with discussing a practical overview of establishing an effective and efficient quality laboratory operation. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/GOOD-LABORATORY-PRACTICE-REGULATIONS-502984/FEBRUARY-2017-ES-TRAININGREGISTRY

This webinar will provide participants with key knowledge of medical device design controls by analyzing FDA 483 observations and learning what the agency is looking for with respect to each design control element.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/DESIGN-CONTROLS-FDA-483-501773/OCTOBER-2016-ES-TRAININGREGISTRY

Enterprise Resource Planning (ERP) software is designed to enhance your business, but not every business is the same. To ensure that you select the right ERP software to obtain the maximum benefits and return on investment for your manufacturing or distribution business, a thorough ERP evaluation process is the key.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ERP-SOFTWARE-MY-ORGANIZATION-501678/SEPTEMBER-2016-ES-TRAININGREGISTRY

This course will cover considerations and requirements when selecting an Electronic Quality Management System (E QMS).Due to the current climate of regulatory compliance there is a need for companies to select the appropriate electronic quality management systems (E QMS).Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SELECTING-E-QMS-SYSTEM-501443/AUGUST-2016-ES-TRAININGREGISTRY

Technical professionals of every stripe are responsible for generating reports. Whether it is policies, procedures, specifications, or analysis, the need to carefully organize documents is essential to the ultimate objective of writing them in the first place. For years, technical writers and administrative professionals have held the keys to easily creating multi-section, easily navigable, numbered and indexed documents.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CREATING-TECHANICAL-DOCUMENTS-NON-WORD-GURU-501537/JUNE-2016-ES-TRAININGREGISTRY

The seminar will begin with an over view of data science and many the steps required for collecting, cleaning, organizing and deriving information out of data. The steps are common to all of the tools and will form the foundation for analyzing, comparing and utilizing the tools used in the remainder of the seminar: R, pandas and Deedle. Topics covered in the foundation are: • Organizing information into data frames • Mutating data frame objects • Indexing data frames • Data alignment between data frames • Handling missing data • Joining data • Reading and writing data from files and databases

MVP Seminars LLC, is a leading nationwide provider of business training seminars at affordable prices, with top-notch providers. Follow-up monitoring program no-charge! Please call 510-558-3495. Largest family run training business in USA.

Dr. Rick Goodman is a professional speaker, motivator, author and training consultant helping organizations Develop Great Leaders - Through Excellence in Communication, Team Building, Change Management, and Customer Excellence. Dr. Rick = RESULTS

Assess change drivers, readiness; Develop effective change initiatives plan; Implement efficient IT best practices; Engage staff; Measure impact on key IT success indicators; Understand impact and benefit; Develop change priority & selection criteria

In this two-day seminar you will receive valuable tools and insights for navigating the most difficult aspects of personal and business evolution.