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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 |
1. EU Medical Device Classification - Webinar By GlobalCompliancePanel
September 17, 2012
Overview: It is not economically feasible to subject all medical devices to rigorous conformity assessment procedures. A more appropriate graduate system is now available that manufacturers should be able to determine the classification of their product early in the development stage. This medical d...
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2. Medical Device Postmarketing Vigilance Reporting: Update and Expectations for Manufacturers - Webin
September 17, 2012
Overview: Major postmarketing vigilance revisions are now in force. A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) came into force on January 1, 2008. Providing more guidance than the previous version, the new document includes new reporting terminology a...
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3. Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
September 17, 2012
Overview: A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA.
There are three types of Premarket Notification 510(k)s that...
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4. Bullet-Proof Closed-Loop CAPA - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: CAPA and the related tools of Failure Investigation and Root Cause Analysis (RCA) is a major tool in product complaint, non-conformance, and OOS failure investigations, and hazard analysis / risk management and mitigation activities.
A compliant CAPA system is required to to "clos...
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5. Computer Systems Used in Clinical Trials - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: This interactive webinar provides an overview of techniques used for buying, deploying, validating, and maintaining computer systems used for clinical trials.
Computer systems used in clinical trials manage enrollment, payments, and collection of subject data. These systems must b...
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6. Root Cause Analysis - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: This course provides clarification of the competencies to plan effective, efficient and thorough investigations and design a process for the successful elimination of recurring failures and deviations.
The material will examine the investigation process from failure identification...
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7. Laboratory Water Systems: Necessary Water Specifications and Validation Challenges -Webinar By Glob
September 11, 2012
Overview: This webinar will assist the attendees in logically investigating and defining the specific quality attributes theirlab water systems need and not just default to manufacturing's required water quality. The need or lack thereof to validate your water system will also be discussed along wit...
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8. Reprocessing REUSABLE Medical Devices - Cleaning & Labeling Requirements -Webinar By GlobalComplia
September 11, 2012
Overview: Much attention has been paid to the regulatory requirements of reprocessing SINGLE use devices. However, there is increasing attention being directed towards reprocessing REUSABLE medical devices and regulatory requirements. The purpose of this seminar is to explain the rationale, the lega...
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9. Residual Moisture Testing - Proven Techniques - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: Monitoring and controlling residual moisture in powders, lyophilized solids, foods, etc can be a critical factor in achieving and maintaining quality products throughout their expected shelf life. Improper levels of moisture in products can result in poor powder flow properties, spoilage, ...
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10. Avoiding 483 Observations and Warning Letters - Webinar By GlobalCompliancePanel
September 11, 2012
Overview: U. S. FDA-regulated companies are responsible for understanding current Good Manufacturing Practices (cGMPs) as defined in the Code of Federal Regulations ( 21 CFR Part 111, 210/211, and 820). They are then required to translate those regulations into procedures and work instructions. Many...
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