Séminaire en ligne, webinaire - États-Unis

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1
Change Management System
07 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Control Management, Management Systems, FDA, Validation Systems
Identifiant de l'évènement:
1333670
2
Implementing an Effective CAPA System
10 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Quality Management System, CAPA, Root Cause Analysis, FDA, Online Training
Identifiant de l'évènement:
1333746
3
Writing Excellent SOPs
10 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Quality System Regulation, Standard Operating Procedures, Quality Management Systems, Online compliance Training
Identifiant de l'évènement:
1333690
4
FDA's Problem with Software Monsters
13 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
FDA Guide Lines, Malware Protection, Compliance Training, Learn about Ransomware
Identifiant de l'évènement:
1333755
5
2-Hour Virtual Seminar on The 6 Most Common Problems in FDA Software Validation and Verification
15 avr 2020 • United States, États-Unis
Organisateur:
Compliance4all
Résumé:
This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
North America Free Trade Agreement, USMCA, Tariffs, Online Compliance Training
Identifiant de l'évènement:
1336107
6
Root Cause Analysis for CAPA
20 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
FDA Techniques, Root Cause Analysis, CAPA System, Online Webinar Training
Identifiant de l'évènement:
1333787
Sujets apparentés:
7
Responsibility for Off-label Claims in Social Media
22 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Role Of Social Media, Off-label Use, FDA, Online Training
Identifiant de l'évènement:
1333720
8
Risk-based Computer System Validation; Reduce Costs and Avoid 483
22 avr 2020 - 23 avr 2020 • Virtual Training Through WebEx, États-Unis
Organisateur:
Complianceonline
Résumé:
This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments. It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
Contact:
Tél.: [+1-888-717-2436];     Email.: referral@complianceonline.com
Sujets:
computer systems validation, computer systems validation training, computer systems validation seminar, csv seminar, computer system validation compliance, computer systems validation regulations, computer systems validation courses, computer systems validation fda, compliance online software training, computer systems validation class room training in the united states
Identifiant de l'évènement:
1345660
9
21 CFR Part 11 Compliance for SaaS/Cloud Applications
22 avr 2020 - 23 avr 2020 • Virtual Training Through WebEx, États-Unis
Organisateur:
Complianceonline
Résumé:
This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments. It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
Contact:
Tél.: [+1-888-717-2436];     Email.: referral@complianceonline.com
Sujets:
21 cfr part 11 compliance
Identifiant de l'évènement:
1345670
10
GMP Expectations for Products Used in Early Phase IND Studies
23 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Gmp Guidelines, FDA, Online Webinar Training, Exploratory IND studies, Quality Systems
Identifiant de l'évènement:
1333807
Sujets apparentés:
11
Excel Spreadsheets - Step-By-Step Instructions for Ensuring Data Integrity
06 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Training On Excel Spreadsheets, Data Integrity, GxP, Online Compliance Training
Identifiant de l'évènement:
1338187
12
Batch Record Review and Product Release
07 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance.A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc. This webinar will analyze each of these necessary elements of the batch record review process.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Process Controls, Batch Record Review, Online Compliance Training, Regularity Requrirements, Batch Record Process
Identifiant de l'évènement:
1341561
13
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Files , Design Dossiers - The Requirements
12 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Required and desirable contents will be discussed.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Device Master Records, Design History Files, FDA, European Union Regulatory Requirements, Design History File, Management
Identifiant de l'évènement:
1338196
14
The Use of Statistical Process Control (SPC) Using Control Charts to Maintain Compliance in the Laboratory
13 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
Attend this webinar to learn how to understand control charts and their underlying statistics, how to choose variables to monitor, how to maintain the records and to plan adjustments.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Control Charts, Statistical Process Control, GLP, Online Compliance Training
Identifiant de l'évènement:
1338151
15
ISO 45001: What is Emergency Preparedness and Response?
15 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
With any occupational health & safety management system (OHSMS) you will have identified potential problems that could occur, and you will need to plan a response so that you can quickly react to these emergencies.This webinar will discuss these plans in detail so that you can not only meet the requirements of the Iso 14001 standard, but also reduce your OH&S impact when problems occur.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
safety management system, Emergency Response Plan, Occupational Health, ISO 45001, Online Compliance Training
Identifiant de l'évènement:
1341618
16
Supplier Auditing for Medical Device Companies
18 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Quality Management Systems, Auditing, Online Training, Purchasing Controls, Medical Device
Identifiant de l'évènement:
1338194
17
Implementation and Management of GMP Data Integrity
20 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition applies to data recorded in electronic and paper formats or a hybrid of both.To assure the quality of raw materials, in process materials and finished goods,laboratory data integrity is assuming greater importance in current Good Manufacturing Practices (CGMP) for US Food and Drug Administration (FDA)-regulated industry. Data integrity and security infractions are not only 21 Code of Federal Regulations (CFR) Part 11 issues but also severe CGMP violations.
Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Data Integrity, Good Manufacturing Practices, FDA, Online Webinar Training, CGMP, Medical Devices
Identifiant de l'évènement:
1341615
18
Issues in Calibrations and Accuracy in Method Validation
26 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
This webinar will cover validation of calibrations and the strengths, weaknesses, and appropriateness of the different types of standards. Without accuracy, a result is not acceptable.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Calibrations, Method Validation, Online Webinar Training, Management
Identifiant de l'évènement:
1338259
19
ISO 14001: What is Emergency Preparedness and Response?
29 mai 2020 • online, États-Unis
Organisateur:
Compliance4all
Résumé:
With any environmental management system (EMS) you will have identified potential problems that could occur, and you will need to plan a response so that you can quickly react to these emergencies.This webinar will discuss these plans in detail so that you can not only meet the requirements of the Iso 14001 standard, but also reduce your environmental impact when problems occur.
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Training On ISO 14001, environmental management system, Emergency Response Plan, Regulatory Compliance Training
Identifiant de l'évènement:
1341628


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Dernière mise à jour: 03 Avril 2020