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Author: charles ben
Company: globalcompliancepanel
Region: USA
Website: www.globalcompliancepanel
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.
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| Articles by charles ben |
1. European Union Filings and Registrations - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: This session covers the various licensing methods (for Drugs, Biologics & Combination Products) by which applicants can file for product licenses (Marketing Authorizations) in one or multiple Member States, as well as fully across all Member States of the European Union. This course specif...
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2. Process Validation Principles and Protocols for Medical Devices - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: The benefit of a consistent process is that the yield meets expected criteria. Firms that are able to implement such processes minimize their process rejections and therefore maximize profit.
Domestic and international regulations actually assist in this endeavor, by setting forth...
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3. Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates f
October 23, 2013
Overview: This 90 minute live, interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations. We will also cover what qualifies a material as a dietary ingredient, considerations ...
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4. Clinical Trial Applications in Canada, and Comparison to the US and Europe - Webinar by GlobalComp
October 23, 2013
Overview: This topic will cover the regulatory submission required in Canada (Clinical Trial Application) and comparison to Clinical Trial Applications in Europe and Investigational New Drug Submissions in the EU. Also covered will be the submission of documentation to Institutional Review Boards, t...
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5. Medical Device Tracking: Latest FDA Update and Expectations - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the event a device presents a serious risk to health that requires prompt attenti...
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6. Medical Device Cleanliness: When and How to adjust LIMIT VALUES - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: This webinar will provide valuable guidance to medical device manufacturers on how to establish and justify limit values for cleanliness. There are several techniques that may be used to set these limits, including comparison involving statistics and historical data. Justification techniqu...
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7. GMP Expectations for Products Used in Early Phase IND and IDE Studies - Webinar by GlobalCompliance
October 23, 2013
Overview: This 60-minute webcast on GMP Expectations for Products Used in Early Phase IND and IDE Studies is designed to provide an understanding of the FDA expectations for information to be in place with regard to products and clinical supplies to be used in initial investigational (IND) and inves...
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8. Cleaning Validations Using Extraction Techniques - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: Cleaning validations are an essential step in the medical device development process. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning pro...
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9. Device Changes and the 510(k) - Webinar by GlobalCompliancePanel
October 23, 2013
Overview: The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when one change is major enough to impact safety / effectiveness, or when a series of lesser changes finally reach the "tipp...
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10. Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) - Pri
October 23, 2013
Overview: Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry. Too often, these are cluttered, confusing, and cause many errors due to the...
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