Séminaire en ligne, webinaire - États-Unis

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1
VC Data — Valuable content: Data for quality decisions and user engagement
31 mai 2022 • Delaware,, États-Unis
Organisateur:
VlogBox
Résumé:
In our upcoming webinar, we’ll discuss the strategies that help make targeting more effective, dig deeper into the matter of geo communities and discuss how to reach them. Our third VlogBox Get-Together webinar is about to take place on 31 May, at 12 PM EDT This time Anna McMichael together with experts from IRIS.TV, and Wantent discuss the tools for customer engagement and effective content targeting within the CTV environment.
Contact:
PR manager;     Tél.: [380675959060];     Email.: yana.k@vlogbox.com
Identifiant de l'évènement:
1487643
2
Featured January 2022 Data for AI Presentation by Ella Hilal, Director of Data Science at Shopify!
01 jui 2022 • Washington D.C. - online, États-Unis
Organisateur:
Cognilytica
Résumé:
The Data for AI Community is geared toward innovative companies pushing the boundaries of what’s possible with Artificial Intelligence and cognitive technologies. This community is focused on the data side of AI including: Data Engineering, Data Preparation, Data Labeling & Annotation, Sourcing and Generating Data, and All Other Topics Data-Related for AI. Join us at this monthly event for high-quality content with compelling & informative speakers and opportunities to network and connect with fellow like-minded individuals.
Identifiant de l'évènement:
1434970
3
Modern Data Strategy and Architecture – How Hanover is Designing for the future
02 jui 2022 • Online Event, États-Unis
Organisateur:
Cognilytica
Résumé:
The June 2022 Enterprise Data & AI event is hosting featured guest speaker Srinivasan Sankar, Enterprise Data & Analytics Leader at the Hanover Insurance Group and his presentation ‘Modern Data Strategy and Architecture – How Hanover is Designing for the future’ on Thursday, June 2, 2022 from 11:30 AM - 1 PM ET!

Accelerating Digital Transformation with the ability to run analytics on all structured and unstructured data, no matter where or in what format that data resides is more important than ever. The pandemic has altered customer and organizational behavior dramatically, forcing digital transformation across multiple industries. Architecting information for the future will create new revenue streams, removing technological barriers, and driving innovation at the world’s leading organizations. Join this engaging and interactive session to learn about Hanover’s data strategy, data architecture, plans for digital transformation and stick around for Q&A with Srinivasan at the end!

Identifiant de l'évènement:
1487302
4
Lessons Learned from Automation Success: Identifying What and When to Automate
23 jui 2022 • Online Event, États-Unis
Organisateur:
Cognilytica
Résumé:
Cognilytica is hosting Kathleen Walch and Ron Schmelzer, Managing Partners at Cognilytica and their presentation ‘Lessons Learned from Automation Success: Identifying What and When to Automate’ on Thursday, June 23, 2022 at 11:30 AM ET! Join this first webinar in the “Advanced Process Management: From Automation to Intelligence” series as Cognilytica managing partners Kathleen Walch and Ron Schmelzer lay the frameworks and questions you need to answer to get started on your Automation to Intelligence journey.
Identifiant de l'évènement:
1487367
5
Intro to CPMAI Methodology for Team Leaders
30 jui 2022 • Online Event, États-Unis
Organisateur:
Cognilytica
Résumé:
Cognilytica is hosting Kathleen Walch and Ron Schmelzer, Managing Partners at Cognilytica and their presentation ‘Intro to CPMAI for Team Leaders’ on Thursday, June 30, 2022 at 11:30 AM ET!

This session will walk through the Cognitive Project Management for AI (CPMAI) methodology to provide team leaders with the foundation needed for project success, especially as they incorporate advanced analytics and AI projects. The CPMAI methodology is the established best practice for AI & ML projects, and increasingly will be demanded by organizations and agencies that plan to develop, procure, and deliver AI and advanced analytics projects. In this session, we will provide real world examples of how CPMAI methodology allows team leaders at organizations to bring their team up to speed on terminology and make sure team members are all in alignment to be more successful and competitive in their AI and big data project efforts.

Identifiant de l'évènement:
1487399
6
Using Learning Management Systems (LMS) to Develop Pharma Training: Rewards & Challenges
21 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

Learning Management Systems (LMSs) are important tools for assuring and demonstrating that Pharma employees maintain their training, and their GMP compliance, up to date.

They often boast great functionality but also have limitations that must be overcome for a Pharma company to use them effectively. An area that is not understood well is the development of training curricula in these systems, which presents its own unique challenges and takes far more time to implement than is commonly thought.

In addition, many employees have these responsibilities in addition to others not necessarily related to training and do not have the luxury of time to create and maintain a complex array of curricula.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368599
7
Hazardous Material Release Reporting Requirements
22 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

Hazardous materials pose a danger to the environment. Federal regulations require immediate reporting to specific agencies (federal and local) in the event of a release to the environment.

We will cover the diferrent requirements, how to determine if you are required to report a release, and strategies to implement proactive actions to minimize the likelihood of a release, and you internal response time to avoid or minimize any potential enforcement actions.

Why you should Attend: The inspection requirements of the SPCC rule are designed to detect oil leaks, spills, or other potential integrity or structural issues before they can result in a discharge of oil to navigable waters of the U.S. or adjoining shorelines.

Regularly scheduled inspections, evaluations, and testing of bulk oil storage containers by qualified personnel are critical parts of discharge prevention. A container integrity inspection and/or testing program may involve one or more of the following: an external visual inspection of containers, foundations, and supports; non-destructive testing (examination) to evaluate integrity of certain containers; and additional evaluations, as needed, to assess the containers’ fitness for continued service.

The type of inspection program and its scope will depend on site specific condition and the application of good engineering practices and this can be accomplished by following applicable industry standards.

Areas Covered in the Session:

Reportable Quantities

CERLA Releases and Reporting

Harmful Discharges under the CWA

EPCRA Release Reporting

Chemical Safety Board (CSB) New rule

Who Will Benefit:

Environmental Managers

Environmental Supervisors

Environmental Technicians

EHS Managers

EHS Supervisors

EHS Technicians

Speaker Profile

Robert A. (Bob) LaRosa, PE, is an environmental engineer and regulatory compliance specialist with more than 30 years’ experience supporting clients in the federal government and in a variety of industries, including chemical, petroleum, transportation, telecommunication, food processing, pharmaceuticals. He has developed and implements SPCC plans at more than 100 different facilities in the transportation, industrial, commercial and government sectors.

As a licensed Professional Engineer, Bob reviews and approves release reporting plans for his clients. Bob is an effective and practiced instructor, with experience delivering more than 60 courses to nearly 1,000 students.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368545
8
Equipment Validation, Tracking, Calibration and Preventive Maintenance
23 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

FDA and EU regulations require that firms have a program for the calibration and maintenance of test and measurement equipment.

The program must include: intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that the equipment does not meet established requirements.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368579
9
21 CFR Part 11 - Compliance for Electronic Records and Signatures
29 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security.

Procedures for controlling electronic signatures and electronic records as described in the FDA Guidance will be explained.

FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being compromised with possible resulting harm to the patient. FDA has set up regulations that address both data security and patient safety. We will show how 21 CFR part 11 considers both.

The confusion over the original FDA regulation and its subsequent "selective enforcement" will be explained. FDA requirements for 21CFR Part 11 validation will be explained. the requirements are composed of technical and procedural aspects. open, closed and hybrid (paper and electronic) systems will be explained.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368569
10
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
30 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers developing these arrangements together.

Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers.The root of many of the problems lies in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues. Part of these arrangements typically involve the development, support and updating of confidential technical files (Drug Master files) which allow suppliers to protect their confidential product and process information from each and every customer and share it only with the Agency.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368521


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Dernière mise à jour: 18 Mai 2022