Article

Microplastics and Water for Injection (WFI)

Microplastics in drinking water and global water sources has been a recently growing topic among scientific research and environmental news. Read more on how this could be effecting the pharmaceutical industry and see it from their perspective.
November 9, 2018
Juha Mattila

Key Takeaways:

  • Microplastics in drinking water raise concerns for pharmaceutical water systems.
  • WFI is filtered and distilled, but no standards exist for microplastic limits.
  • RO membrane filtration is the best pre-treatment for microplastic removal.
  • Distillation methods help eliminate non-condensable particles and pyrogens.
  • Regulators may need to update pharmacopeial standards for microplastic risks.  

STERIS Finn-Aqua experts, have written "Microplastics and Water for Injection (WFI)". 

Microplastics in drinking water and global water sources has been a recently growing topic among scientific research and environmental news. The presence of microplastics in the environment and the current lack of regulation around them raises concerns about plastics going into humans via our digestion system and similarly polluting all types of life forms in our seas, rivers and lakes. Read more on how this could be effecting the pharmaceutical industry and see it from their perspective.

Suggested Content

Technical Tip

Critical Process Parameters

When developing a cleaning process, it is important to consider various factors related to the surface, process cleaner, and cleaner.
Article

The Cost of Microbial Control

The pharmaceutical industry is facing pressure to continuously challenge and improve its manufacturing processes to achieve regulatory compliance and produce high quality product. New technologies to improve microbial control, support root cause investigation and provide faster response are expected to become available over the next few years. 
Technical Tip

Introduction to Regulatory Resources

Government regulatory agencies and industry organizations develop guidelines to ensure pharmaceutical and biotechnology manufacturers have robust cleaning processes. This article will provide an overview of resources related to cleaning validation in the pharmaceutical and biotechnology industries.
1 of 3

You're leaving this site.

You are being redirected off of the STERIS Life Sciences website. If you wish to continue, click "Leave STERIS Life Sciences". Otherwise, click "Take Me Back".