Home
Categories
Pharmaceutical
Hi Tech Manufacturing
Food
Finance
Design & Build
Containment
Cleaning
Sustainability
HVAC
Personal Protection
Regulatory
CT CONFERENCE
Company News
Events
Directory
Search
Close search
Home
Company
RAPS Regulatory Affairs Professionals Society
RAPS Regulatory Affairs Professionals Society
Activities:
Regulatory
X
LinkedIn
Trending Articles
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
Identifying and preventing contaminant leakage from your cleanroom
A common solution to machinery contamination in a cleanroom is to build a cleanroom within a cleanroom using partitions or curtains, to isolate the machine. Chris Lindlar from...
Integrity testing of HEPA filters: A practical approach
Filtering the air in aseptic process areas is critical to maintaining the cleanliness of the production environment. Jesus Casas provides tips to ensure HEPA filters are fit...
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...
Legionella testing: Modern alternatives to the ‘gold standard’ test
The development of significantly faster, more sensitive testing protocols provide more options for detection Legionella than the complex plate culture test, but these also have...
Upcoming event
Clinical Pharmacy Congress
10-11 May 2024 | Conference | London, UK
See all
Related Content
Regulatory
Euro Convergence 2020 Live Online new dates
26–30 October 2020 | Virtual event
Regulatory
USP and British counterpart join forces
Pharmacopoeias in the US and in the UK have signed a memorandum of understanding to strengthen quality standards for medicines
Regulatory
RAPS Europe Conference 2019 to address sweeping changes in European regulatory environment
The event in May comes as a host of new laws affecting the medicines, medical devices and <em>in vitro</em> diagnostics (IVDs) sectors are due to come into effect
RAPS Regulatory Conference – Europe 2019
13-14 May 2019 | Brussels, Belgium
Regulatory
Survey of regulatory professionals highlights lack of understanding of new MDR rules
A survey of more than 200 regulatory professionals has revealed a lack of understanding of the new Medical Device Regulation (MDR) requirements
Regulatory
RAPS publishes compensation survey of regulatory professionals
Offering a look at how much healthcare product regulatory professionals earn, which products they work on, what their work entails and how their roles have evolved
Regulatory
Workshop focuses on changes to MDR
The event will take place in Brussels on 20 November 2018 hosted in collaboration between RAPS and TOPRA
Subscribe now