About me
Dr. Erich Travniczek

My Passion Is Your Benefit

30

years of world-wide regulatory affairs

15

years activity as Qualified Person for registered drugs and investigational new products

6

years in manufacturing and control for biological and biotechnological medicinal products and support in pharmacovigilance, development, change control and agencies-presentations.

My Experience For Your Business

- Qualified Person
- GMP Related Activities
- SOP
- Change Control
- Regulatory Advice

My Education & Business Life

Study of „classical biology“
PhD with a doctoral thesis about Herpes Simplex Virus and Transformation of Cells
 
  • – Manufacture and analysis of bacterial vaccines
  • – Manufacture of bacterial diagnostics
  • – Manufacture and release of hemostasis proteins
  • – Regulatory affairs world-wide
  • – GMP Audits
  • – Batch Release
  • – GMP-confirmations for EU-drug submissions
  • – Industrial Manager (formerly License Holder for a pharmaceutical company)

Contact Me For More Information!