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What is ISO 8 cleanroom classification?
Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
Impact of the new Annex 1 on sterile filling in pharma
EU GMP Annex 1 is a whole new era for the sterile filling industry. From barrier technology to “first air”, pharmaceutical manufacturers have a lot to decide. Johannes...
Danish pharmacies invest in hi-tech environmental monitoring system
The construction of a new building prompted one of Denmark’s largest pharmacy businesses to invest in Vaisala’s viewLinc Continuous Monitoring System (CMS) to protect the...
Industry 4.0: What is the advantage of real-time digital signage?
Olivia Fernandez from Digital Therapeutics (DTx) disusses how digital signage can serve in cleanrooms as a versatile and powerful tool that allows those in charge to ensure...
Scientific justification for monitoring indirect product contact surfaces
Findings from a survey on several pharma companies unveil the best practices for monitoring indirect product contact surfaces. Walid El Azab and Lillia Belkhamassi explain
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Clinical Pharmacy Congress
10-11 May 2024 | Conference | London, UK
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Manufacturing
Big names announced for leading Pharma and Cleanroom conference
The Cleanroom Technology Conference and Manufacturing Chemist Live collaboration will take place on the 10-11 November. Delegate tickets are currently available
Regulatory
NSF launches programme to comply with water fittings regulations
Certification enables food equipment manufacturers to demonstrate compliance with UK regulations
Manufacturing
NSF debuts validation services for hemp and hemp-derived CBD
The NSF subsidiary Quality Assurance International (QAI), a USDA-accredited organic certifier, will now offer the services
Regulatory
NSF Responsible Person Course gains MHRA recognition and Cogent Gold Standard
The Responsible Person (import) is required to implement a system for confirming QP certification has taken place when importing medicines from the EEA into the UK
Manufacturing
NSF to host pharma training across Europe
In September there will be courses in the UK, Italy and Ireland
Regulatory
NSF Webinar: Introduction to the GMP Standard for OTC Drug Manufacture
23 July 2019 | Free Webinar, 11.00am ET US Eastern time | Duration: 30 minutes
Regulatory
NSF takes the stage at MedTech Forum
At the panel session <em>Notified Bodies: A Key Pillar of the New EU Regulatory System</em>, Robyn Meurant described NSF’s experience as a potential new notified body
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