World Conference Calendar

33842 Conferences

Best Practices for Global Regulatory Intelligence: Dos and Don'ts

Added by OCPcompliance on 2014-12-04

Conference Dates:

Start Date Start Date: 2015-01-15
Last Date Last Day: 2015-01-15
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2015-01-14

Conference Contact Info:

Contact Person Contact Person: David Jonathan Moses
Email Email: onlinecompliancepanel@gmail.com
Address Address: 38868 Salmon Ter, Fermont, California, 94536, United States
Phone Tel: 5105099659

Conference Description:

Description:
This webinar is intended to help you get familiarized with the best practices for global regulatory intelligence including dos and don'ts. This webinar is further intended to increase our awareness for the importance of implementing a holistic global regulatory intelligence program suitable for your medical product types.

It is believed that actionable and practical regulatory intelligence can help an organization save a significant amount of resources (time, efforts and financial). Thus, it is imperative we become aware of and get familiarized with the best practices for developing a global regulatory intelligence program. This webinar will address the best practices for you to take action, significantly benefiting your organization in many ways.

Why Should you Attend:
Attend this webinar to adequately develop and implement a holistic global regulatory intelligence program.

Objectives of the Presentation:
The key objectives of the presentation are to give better insight on:
Applicable Laws and Regulations
Guidance, Rules, and Standards
Regulatory Intelligence for Drugs, Biologics, Biosimilars, and Medical Devices including In Vitro Diagnostic Medical Devices (IVDs)
What Is Important to Consider?
R&D, Patenting (IP) and Applicable Regulatory Pathways
Questions and Issues to Identify and Address
Totality and Flexible Approaches
Interfacing: Roles and Benefits
Reimbursement Issues: What, When, Why, and How
Intellectual Property (IP) Issues
Alignment between Regulatory Plan/Strategy, Reimbursement, and IP
New Requirements to Integrate: Risk Management Plan (RMP)/Pharmacovigilance (PV)
FDA Unique Device Identification/Identifier (UDI)
Detailed Contents
Common Mistakes Leading to Serious Consequences (Patient Safety and Business Operations)
Practical, Actionable, and Sustainable Solutions (PASS)
Speaker's Experience and Actual Cases
Who can Benefit:
Regulatory Affairs
Management: CEOs, VPs
R&D and Product Development
Legal Counsel and Compliance Officers
Marketing
Clinical Affairs
Consultants
Contractors/Subcontractors
Other Interested Parties
About Company:

Online Compliance Panel creates and delivers comprehensive industry relevant training sessions. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Live interactions on compliance training make the process holistic and effective. Online Compliance Panel largely emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices and market trends.

We strive to incorporate high standards in developing a culture facilitating exchange of ideas resulting in functional excellence. Online Compliance Panel believes in nurturing ideas and thought processes through innovative e-learning methodologies. Our products and services are designed to offer customized solutions to industry and market. We bridge the gap between experience and knowledge thus delivering original and creative content.

Our objectives of employing interactive mediums ensure effective communication and mutual exchange of ideas. Online Compliance Panel closely follows best practices and regulatory trends in the global compliance scenario. We also observe and communicate trends witnessed in FDA, ISO regulations, process and design validation. All updates and additions to important laws can be accessed by our customers in real time.

Contact:
Toll free: +1-510-857-5896
Email: webinar@onlinecompliancepanel.com
OnlineCompliancePanel LLC,
38868 Salmon Ter,
Fremont, CA 94536, USA
Use For Registration: http://bit.ly/dontanddo
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