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Author: Webinar Web
Company: GlobalCompliancePanel
Website: www.globalcompliancepanel.com
Author Comment / Biography:
GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.
GlobalCompliancePanel offers a broad range of channels for broadcasting and exchange of information through web based training, web alerts & discussion forums.
GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management. Apart from providing excellent training to compliance professionals by compliance & consulting experts, GlobalCompliancePanel would also focus on providing:
Information to ensure compliance and enhance quality with regulations for individuals as well as the organizations Latest updates on industry trends, industry best practices and any modifications in the regulatory affairs One stop destination for all your queries and to share and discuss issues, ideas and best practices and A resource on the data sheets, whitepapers, articles, books on industry standards, training kits, software tools, insights, press releases, etc on governance, regulatory, compliances and quality management across different industries.
GlobalCompliancePanel plays a role of bringing together the regulators or experts on regulation with the community who needs to learn or be aware of those regulations. GlobalCompliancePanel is started with the goal to create an excellent interactive platform for the experts and the user community thereby making costs of training more affordable with increased convenience.
GlobalCompliancePanel strives to understand the changing customer needs and enrich their quality of life by simply providing world-class training to increase their productivity and professional growth. Global Compliance Panel enables the companies in triggering business processes through regulatory notifications and industry alerts.
NetZealous LLC DBA GlobalCompliancePanel is headquartered at 1000 N West Street | Suite 1200 | Wilmington | DE 19801.
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| Articles by Webinar Web |
11. 21 CFR Part 11: Ins and Outs of Audit Trails - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: Audit trails are major requirement for many software applications regardless of an industry or users. This is especially true when it comes for Pharma and medical devices companies and other businesses that have implemented or are planning on implementing 21 CFR Part 11 and striving to com...
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12. Creating Material, Waste, and Personnel Flow Diagrams for Cleanrooms and Controlled Environments -
September 11, 2012
Overview: This live webinar concentrates on identifying and discussing flow requirements associated with cleanrooms.
We will explore the typical flows used in cleanrooms and controlled environments for material, waste and personnel. The webinar also discusses implementation and management o...
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13. Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical Fi
September 11, 2012
Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical File (TF). Do you know what inform...
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14. Calibration and Assuring Accurate Measurements - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: Purpose of this training to vaccinate the organization against common calibration and measurement related problems to minimize future variation, scrap and/or complaints, including practical advice on how to assure data accuracy and prevent measurement problems.
Areas Covered in th...
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15. Developing and Maintaining Pre-marketing Master Regulatory Files - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: This webinar will review the different types of master regulatory files necessary for demonstration of compliance with GXP procedures, providing the regulatory authorities with appropriate data, and maintaining a well organized source/support documentation.
Each submission to the ...
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16. Safety Critical Software - Software Risk Management - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: Using IEC62304 as the internationally recognized software lifecycle standard the risk dependent activities and documentation requirements will be explained. Questions like:
How much detail is required in the requirement specification?
What is a software unit?
How...
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17. Selling Medical Devices in the EU-Medical Device Directive, CE & FDA -Webinar By GlobalCompliancePa
September 11, 2012
Overview: Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted into the 29 member countries comprising the EU. The market popul...
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18. China: Compliance Processes for Life Science Products: Company Establishment, Clinical Trials, Regi
September 11, 2012
requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products. Why should you attend: China has been improving its regulatory regime governing the food and pharmaceutical industry in recent years. In 2010, by promulgating ...
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19. Improving Constraint Performance - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: Many times, when applying Theory of Constraints (TOC), a constraint is assumed to be a fixed entity and the efforts are focused elsewhere on ensuring that the constraint is given the highest priority. However, an often-overlooked opportunity is to "chip away" at the constraint by moving so...
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20. 510(k) Preparation, Submission, and Clearance - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: This webinar is intended to demonstrate how to prepare a 510(k) in an adequate manner with increased quality for submission and subsequent clearance.
The section [510(k)] of the Federal Food, Drug, and Cosmetic Act (FD&C Act or the Act) describes the premarket notification require...
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