Keep my session open?
Ending In 
The session is expired
Your session has expired. For your security, we have logged you out.
Would you like to log in again?

Quality assurance considerations in single-use manufacturing

Quality assurance considerations in single-use manufacturing
How, as a manufacturer of single-use systems, we support biopharmaceutical companies in implementing single-use technologies that reduce contamination risk, improve resource efficiency and lower labour and energy costs.

Today the single-use manufacturer is faced with unique challenges in fulfilling the expectations of its biopharmaceutical customers, and the regulators who are applying ever-expanding controls over this emerging industry. Many of these challenges directly impact the quality and regulatory compliance organisations within the single-use manufacturing organisation. The attached article provides a discussion of the quality and regulatory foundations upon which VWRs 'best-in-class' single-use manufacturing is based. The considerations include, but are not limited to:

  • Cleanroom certification and contamination control
  • Environmental monitoring
  • Sterility and sterile-barrier packaging validation