Master Soil Selection for Cleaning Validation of Parts Washers

About the Author

Technical Services Senior Manager

Steris Corporation

Paul Lopolito is a Senior Technical Services Manager for the Life Sciences Division of STERIS in Mentor, Ohio. He currently provides global technical support related...

Olivier Van Houtte

Senior Marketing Manager

STERIS

Olivier Van Houtte is a Senior Marketing Manager in the Life Sciences Division of STERIS. Olivier holds a bachelor’s degree in business-marketing from Quebec University...

Dijana Hadziselimovic

Technical Services Laboratory Specialist for the Life Sciences Division

STERIS Corporation

Dijana provides technical support in the area process and research cleaners and conducts laboratory experiments to recommend cleaning procedures and field support. She has over...

Si Myra Tyson

Technical Service Associate

STERIS

Si Myra Tyson is a Technical Service Associate for the Life Sciences Division of STERIS. She currently conducts laboratory evaluations to recommend cleaning procedures for...

Technical

Selection Criteria for Pharmaceutical Containment Equipment

1 March 2024

Pharmaceutical manufacturing facilities produce a variety of products, including highly potent products that require safety measures to prevent adverse health effects on patients and operators. To ensure safety, these facilities use containment equipment to minimize the risk of contamination. This article presents criteria for selecting containment equipment, considering both...

Technical

A Sustainable Approach to Steam Quality Management

1 March 2024

The world is beginning to grasp the huge challenge of achieving net-zero carbon emissions, or carbon neutrality, by 2050. Many countries have committed to achieving this ambitious goal. As a major global industry, the pharmaceutical sector has a significant role to play. For thermal energy–intensive industries, such as pharmaceutical manufacturing, the long-term future options to maintain...

Technical

Concluding Compliance Challenges with Validation 4.0

13 March 2024

As the pharma industry moves to an ambitious Validation 4.0 paradigm, computerized systems play a pivotal role in enabling the rapid transition. Innovation and agility in computerized system validation (CSV) received a strong push in the second half of 2022 with the publication of the FDA draft guidance on “Computer Software Assurance for Production and Quality System Software”

About the Author

Facilities of the Future: Meeting the Demands of Breakthrough Therapeutics

Emerging Leader Hacker to GAMPer in 10 Weeks

New Initiative Seeks to Back up ICHs Harmonization Mission

Data Science-Assisted Biopharmaceutical Tech Transfer and Process Characterization

Entering a New Era of Innovation and Collaboration With the Focus on the Workforce of the Future

Q&A with ISPE Foundation Professional Development Grant Recipient Silas Tamufor

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