Back to Standards for Immunohematology Reference Laboratories, 10th Edition – Portal
Standards for Immunohematology Reference Laboratories, 10th Edition – Portal

Standards for Immunohematology Reference Laboratories, 10th Edition – Portal

    Product Code: 173125SP
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Standards for Immunohematology Reference Laboratories, 10th Edition – Portal
  • List Price: $152.00
  • Member Price: $126.00
 
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Back to Standards for Immunohematology Reference Laboratories, 10th Edition – Portal

Product Features:

Multi-user access is available for this product at a discounted rate. For details on the discount(s), please see below. The 10th edition of Standards for Immunohematology Reference Laboratories, effective January 1, 2018, relies on a matrix of quality management system and detailed operational requirements, such as those defining minimum antisera resources.

The Standards Portal allows users to customize their profile based on the activities for which they are accredited and can be rearranged at any time. Standards that do not apply to a user’s profile will appear grayed out to ensure that purchasers are aware of the standards that apply to their facility and those that do not.

The Standards Portal is also fully searchable by key word, chapter, or standard number, allowing users to navigate quickly to the most relevant standards to them at that time. Guidance is provided on how to implement a standard, why it was created, or why a change was made from this edition to the last. Any relevant documentation that would assist users in implementing the standard in question is provided.

New Benefits to Users

All links to outside websites and cross references to other standards in the portal are live and appear in popup windows to allow users to be able to see both the standard in question and the linked post. The full edition of the IRL Standards (not including any guidance) is printable at any time to ensure that users can take the IRL Standards on the go.

Any interim or emergent standards will appear seamlessly in the portal once effective and highlighted.

By purchasing the Standards for Immunohematology Reference Laboratories, 10th edition (“Standards”) through the AABB Standards Portal (“Portal”), users acknowledge and agree that they will access the Standards solely for their own personal and/or professional use and not distribute, copy, or provide access to the Standards for use by any third parties. Furthermore, users will securely maintain their login and password for the Portal. In the event that AABB or its authorized agents discover that users have not complied with these Terms and Conditions of Use, they understand that they will lose all rights to access the Standards and will not be entitled to any refund.

Significant changes in the 10th edition include:

  • A new standard, 1.3.1, has been added allowing for there to be exceptions to existing policies, processes and procedures on a case by case basis with the approval of the laboratory director.
  • A new standard, 2.3, requires that all laboratories have a written plan for the implementation of allele determinations for RHCE variants.
  • Standard 4.1.2.2 is new and has been included to allow facilities located outside of the United States to use testing centers in their country that have been approved by their Competent Authority.
  • A new standard, 5.1.5.2.1, requires that laboratories who receive oral requests for blood components are recorded and maintained.

Multi-User Access Fees

Units Purchased

Cost per Portal Unit (Member Price)

Cost per Portal Unit (Non Member Price)

1-5

$126

$152

6-10

$111

$137

11-15

$96

$122

16 +

Contact Customer Support for pricing

Contact Customer Support for pricing

For more information about purchasing multi-user access please contact:

AABB Customer Support
4550 Montgomery Avenue
Suite 700, North Tower
Bethesda, MD 20814
Phone: +1.866.222.2498
+1.301.215.6489
Fax: +1.301.951.7150
Email: sales@aabb.org

When purchasing multi-user access, you will be asked to assign access to specific individuals.

(2017, AABB)

Effective date: Effective date: January 1, 2018

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