OR WAIT null SECS
MJH Life Sciences
Jennifer Markarian is manufacturing reporter for Pharmaceutical Technology.
October 06, 2015
The challenge of achieving zero visible defects (i.e., particulates) in parenteral drugs will require a coordinated effort at all stages of the supply chain, particularly in the production and filling of primary containers.
October 02, 2015
September 16, 2015
Appropriate cleaning procedures are crucial for any cGMP aseptic or sterile pharmaceutical manufacturing process, including vial filling; operators share best practices for cleaning.
Preventing contamination requires quality systems to be in place, including routine cleaning, a robust cleaning validation program, and preventive maintenance.
September 02, 2015
Operator attention to detail and adherence to procedures are crucial for proper cleaning.
August 19, 2015
Paperless operations improve efficiency and increase assurance of product quality.