New GS1 US Guideline-2013 Drug Supply Chain Security Act

Thursday, Apr 06, 2017 at 11:30AM - 2:30PM
Fremont, CA
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Live Session
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$250.00 $8.62 28

Super Combo Offer
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$500.00 $16.34 20

Special Offer
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$625.00 $20.20 20

Corporate Live Session
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$1,250.00 $39.52 22

Event Details

Description
New provisions of the 2013 Drug Supply Chain Security Act (DSCSA) will come into effect in 2023. The industry is using the newly updated GS1 Guideline to update their systems to comply with the law. There are many new features in the guideline that need to be understood before making changes to existing systems. This webinar will review new materials in the guideline and help you prepare to comply with the 2023 requirements. There are additional requirements that have yet to be decided within the industry that you need to be aware of and follow as they are resolved by industry and the FDA.

Objectives of The presentation
  • Learn why current solutions may not work moving forward
  • Be able to describe what your company needs to do to meet the next set of requirements
  • Understand the suite of standards the industry is using to comply with DSCSA
  • Understand key business processes and how to account for them using the guideline
  • Prepare to be able to respond to trading partner requirements if errors occur
  • Be able to create a RFP for enhancements to your current solution
Why Should you Attend
Members of the US Pharmaceutical Supply chain will begin to use the GS1 EPCIS suite of standards to comply with provisions of the DSCSA law due to be in effect on November 27, 2023. This training will review what is required, timelines for implementation and how to use the GS1 US Guideline to comply and prepare to share serialized data with your trading partners.

Areas Covered
  • Background on DSCSA
  • Past Requirements
  • Future Requirements
  • Industry Challenges
  • Event based architecture
  • Sample events between trading partners
  • Collecting Transaction History back to the Manufacturer
Who will Benefit
  • Regulatory
  • Operations
  • VP or Director of I.T.
  • Persons responsible for licensing/registration
  • Manufacturing and distribution/supply chain
  • Anyone new to the GS1 System of Standards
  • Professionals in Production and Supply Chain
  • Outsourcing Managers
  • Procurement, R&D Managers
For Registration
http://onlinecompliancepanel.com/webinar/NEW-GS1-US-GUIDELINE-506697/APRIL-2017-ES-EZEVENT

Note: Use Promo code DE5YU and get 10% off on registration (Valid till APRIL 30th 2017)

Organization Details

Online Compliance Panel (OCP) 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. OCP 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. OCP 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. OCP 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.

Our mission is to empower compliance professionals through effective online training sessions. Our world class training methodologies stem from comprehensive understanding of client requirements. The content conforming to FDA and ISO standards is developed by well qualified and experienced industry leaders. Our offerings will exceed expectations and add value to your investment.

The content in various categories such as medical devices, pharmaceuticals and biotechnology will raise the bar in terms of quality already on offer .We hope to contribute to the creation of responsible organizations creating benchmarks in quality, integrity and transparency.

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Venue Map (from Google Maps)

Online Event
38780 Tyson Lane, Apt 210
Fremont, CA 94536

Starts April 06, 2017 at 11:30AM - 2:30PM

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Contact Information

Organization: Online Compliance Panel LLC

Event Contact: OCP Panel

Phone: 15108575896