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CSL Behring

Division of CSL Ltd.

Latest From CSL Behring

England's NICE OKs Shire’s Takhzyro For Rare Hereditary Disease

England’s health technology assessment body has recommended the use of Shire’s orphan drug Takhzyro for use in patients with hereditary angioedema, but only in certain circumstances and provided the company offers the product at the agreed discounted price.

United Kingdom Health Technology Assessment

Mustang Bio Joins RMAT List; Eiger Brings Home Its 4th BTD

Gene therapy and lambda interferon products are highlighted in the new Review Pathways section of the US FDA Performance Tracker, which keeps track of breakthrough therapy (BTD), regenerative medicine advanced therapy (RMAT), qualified infectious disease product (QIDP) designations and biosimilar submissions.

Rare Diseases Review Pathway

Grifols Wins Early FDA OK For SCIg Xembify, Setting Stage For Margin Growth

Analysts said Grifols is poised for profit margin growth after the US FDA approved its first 20% subcutaneous immunoglobulin, Xembify, for treating primary immunodeficiencies.

Commercial Companies

US FDA Advertising Citations Remain Rare In 2018

With only seven letters last year, Office of Prescription Drug Promotion appears to be continuing its enforcement retrenchment as agency reconsiders its approach to Rx communications.

Advertising, Marketing & Sales Enforcement
See All

Company Information

  • Industry
  • Pharmaceuticals
  • Therapeutic Areas
  • Non-Specific
  • Alias(es)
  • ZLB Central Laboratory
  • ZLB Bioplasma AG
  • ZLB Behring
  • Ownership
  • Private
  • Headquarters
  • Worldwide
    • North America
      • USA
  • Parent & Subsidiaries
  • CSL Ltd.
  • Senior Management
  • Paul Perreault, CEO
    David Lamont, CFO
    Andrew Cuthbertson, PhD, Dir., R&D & CSO
    Alan Wills, SVP, Strategy & Bus. Dev.
  • Contact Info
  • CSL Behring
    Phone: (41)(610) 878-4000
    1020 First Ave.
    P.O. Box 61501 King of Prussia, PA 19406-0901