Good Manufacturing Practice


GMP, the abbreviation of Good Manufacturing Practice, requires that manufacturers and packagers of APIs and medicinal products take proactive steps to ensure that their products are safe, pure and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mix-ups, and mistakes. The sole intention is to protect consumers and patients from purchasing a non-effective or even dangerous product. Failure of firms to comply with GMP regulations can result in serious consequences, like recalls or withdrawal from the market.

Dr. Ursula Koller

certified EOQ Quality Auditor
and Quality Systems Manager

About us

Our customers

  • pharmaceutical and biotechnology manufacturer
  • pharmaceutical wholesaler and logistic companies
  • blood banks
  • hospitals, and hospital pharmacies

and their suppliers