Cleanroom

Phizzle and GlassHouse Deliver Managed Service to Automate Cleanroom Monitoring

Wednesday, July 21, 2021 - 2:50pm

San Francisco, California--(Newsfile Corp. - July 21, 2021) - Phizzle and GlassHouse Systems of Toronto today announced a managed service offering that provides a flexible way to automate cleanroom monitoring and enable remote, real-time operations of environmental equipment used in R&D and manufacturing cleanrooms by both large and small organizations.

Key Points: 
  • San Francisco, California--(Newsfile Corp. - July 21, 2021) - Phizzle and GlassHouse Systems of Toronto today announced a managed service offering that provides a flexible way to automate cleanroom monitoring and enable remote, real-time operations of environmental equipment used in R&D and manufacturing cleanrooms by both large and small organizations.
  • To view the full announcement, including downloadable images, bios, and more, click here .
  • Phizzle's EDGMaker is the only IoT solution to remotely operate and automate multi-vendor particle counters for scientific data applications.
  • For over 26 years, GlassHouse Systems (GHS) has been designing, implementing and servicing the enterprise IT community with best in class mission-critical infrastructure and professional services.

Summa Equity acquires G-CON Manufacturing, the leading US-based provider of POD® cleanroom solutions

Tuesday, July 20, 2021 - 5:06pm

Through its acquisition of G-CON , Summa Equity enters the rapidly growing biopharmaceuticalmanufacturing market, including cell and gene therapy manufacturing.

Key Points: 
  • Through its acquisition of G-CON , Summa Equity enters the rapidly growing biopharmaceuticalmanufacturing market, including cell and gene therapy manufacturing.
  • STOCKHOLM, July 20, 2021 /PRNewswire/ --Summa Equity Fund II ("Summa") has acquired a majority stake in G-CON, a leading US-based manufacturer of prefabricated cleanrooms used for manufacturing within the pharmaceuticals industry.
  • "We are proudto partner with G-CON for the next, exciting chapter of its growth trajectory," says Marika Viti, Director at Summa Equity.
  • G-CON POD cleanroom units surpass traditional cleanroom structures in scalability, mobility and the possibility of repurposing the PODs once the production process reaches its lifecycle end.

G-CON Manufacturing, the leading US-based provider of POD® cleanroom solutions, is acquired by Summa Equity

Tuesday, July 20, 2021 - 5:05pm

The COVID-19 pandemic has underlined the need for uninterrupted off-site construction of cleanroom infrastructures.

Key Points: 
  • The COVID-19 pandemic has underlined the need for uninterrupted off-site construction of cleanroom infrastructures.
  • "We are proud to partner with G-CON for the next, exciting chapter of its growth trajectory," says Marika Viti, Director at Summa Equity.
  • Summa invests in companies that are solving global challenges and creating positive Environmental, Social, and Governance (ESG) outcomes for society.
  • G-CON POD cleanroom units surpass traditional cleanroom structures in scalability, mobility and the possibility of repurposing the PODs once the production process reaches its lifecycle end.

Quattroflow Increases Single-Use Pump Manufacturing Footprint with Construction of New Cleanroom

Thursday, July 15, 2021 - 9:15pm

Expected to open in October 2021, the additional cleanroom will more than double the Quattroflow cleanroom space in Duisburg, Germany.

Key Points: 
  • Expected to open in October 2021, the additional cleanroom will more than double the Quattroflow cleanroom space in Duisburg, Germany.
  • This investment will help support growing customer demand for single-use pump products used in the production of biologics, drugs and vaccines.
  • The new cleanroom will operate independently from the existing one while following the same assembly procedures to ensure product uniformity.
  • "Expanding our cleanroom footprint is a critical step in increasing our single-use manufacturing capacity to satisfy this growing market demand.

Global $5 Billion Cleanroom Technology Market to 2028: Growing Compliance with Stringent Regulatory Standards for New Product Approvals

Friday, July 2, 2021 - 9:00pm

The global cleanroom technology market size is expected to reach USD 5.0 billion by 2028 and is expected to expand at a CAGR of 5.4% over the forecast period.

Key Points: 
  • The global cleanroom technology market size is expected to reach USD 5.0 billion by 2028 and is expected to expand at a CAGR of 5.4% over the forecast period.
  • Growing compliance with stringent regulatory standards for new product approvals, technological advancements by key players to provide customized services to manufacturing companies and increase in awareness about contamination-free products coupled with growing demand in biopharmaceutical and pharma companies to develop high-quality products are some of the key factors driving the market growth.
  • Moreover, an increase in the development of healthcare facilities and an increase in government initiatives to spread awareness are factors anticipated to drive the market.
  • Thus, a 50% fall in the global production capacity owing to which the exceeding demand is left unmatched has impacted the market in a significant way.

Cleanroom Technology Market Size, Share & Trends Analysis Report 2021-2028 - ResearchAndMarkets.com

Friday, July 2, 2021 - 10:05am

The "Cleanroom Technology Market Size, Share & Trends Analysis Report by Product (Consumables, Equipment), End-use (Pharmaceutical Industry, Medical Device Industry), Region, and Segment Forecasts, 2021-2028" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Cleanroom Technology Market Size, Share & Trends Analysis Report by Product (Consumables, Equipment), End-use (Pharmaceutical Industry, Medical Device Industry), Region, and Segment Forecasts, 2021-2028" report has been added to ResearchAndMarkets.com's offering.
  • The global cleanroom technology market size is expected to reach USD 5.0 billion by 2028 and is expected to expand at a CAGR of 5.4% over the forecast period.
  • Moreover, an increase in the development of healthcare facilities and an increase in government initiatives to spread awareness are factors anticipated to drive the market.
  • Cleanroom Academy, founded in 2008, is an example of an organization dedicated to providing related aids to manufacturing companies to optimize their work processes and training pertaining to this technology.

US LED, Ltd. Launches New LED Flat Panels with Selectable CCT and Wattage Options

Thursday, July 1, 2021 - 3:23pm

HOUSTON, July 1, 2021 /PRNewswire/ -- US LED announces the launch of its L-Grid Edge Xtreme XL Select, a new generation of LED flat panels with selectable CCT and wattage options.

Key Points: 
  • HOUSTON, July 1, 2021 /PRNewswire/ -- US LED announces the launch of its L-Grid Edge Xtreme XL Select, a new generation of LED flat panels with selectable CCT and wattage options.
  • LED flat panels offer versatility for end-users while keeping inventory levels low for distributors and contractors.
  • In addition to being DLC Premium Listed, these flat panels are NSF Certified for controlled environments like cleanroom manufacturing or food processing areas.
  • "It's exciting to be able to add these innovative flat panels to our diverse portfolio of LED lighting solutions," said Ron Farmer, CEO at US LED.

Exacis Biotherapeutics Makes Strategic Investment In Manufacturing by Hiring Head of Technical Operations and Securing Space in a GMP Cleanroom Facility Recently Completed by Factor Bioscience

Thursday, July 1, 2021 - 3:00pm

Exacisis partnering with parent Factor Bioscience toproduce its iPSC-derived CAR-T and NK cells within a GMP cleanroomfacilitybuilt by Factor,and Exacis has hiredBryan Jones PhD as its Head of Technical Operations.

Key Points: 
  • Exacisis partnering with parent Factor Bioscience toproduce its iPSC-derived CAR-T and NK cells within a GMP cleanroomfacilitybuilt by Factor,and Exacis has hiredBryan Jones PhD as its Head of Technical Operations.
  • Exacis' parent company, Factor Bioscience, recently completed construction of a 5,000 square foot GMP cleanroom facility at its Cambridge, Massachusetts headquarters.
  • Exacis will use this new facility to produce its allogeneic mRNA engineered cell-therapy product candidates for non-clinical and clinical testing.
  • Dr. Jones will oversee the buildout of the Manufacturing and Quality Operations working alongside Factor Bioscience in the new facility.

Superior Sensor Technology™ Develops Custom Differential Pressure Sensor for Particles Plus®

Wednesday, June 30, 2021 - 5:23pm

LOS GATOS, Calif., June 30, 2021 /PRNewswire/ -- Superior Sensor Technology today announced that Particles Plus has adopted Superior Sensor's differential pressure sensor technology in their next-generation air quality monitoring instruments for clean rooms and OEM applications.

Key Points: 
  • LOS GATOS, Calif., June 30, 2021 /PRNewswire/ -- Superior Sensor Technology today announced that Particles Plus has adopted Superior Sensor's differential pressure sensor technology in their next-generation air quality monitoring instruments for clean rooms and OEM applications.
  • Particles Plus took advantage of NimbleSense to create a custom differential pressure sensor that incorporates unique features specific to their applications.
  • Particles Plus sells both OEM and private label products and will incorporate Superior Sensor's differential pressure sensor in its 9000 and 2000 series products for cleanroom applications and future indoor air quality and ambient air quality product applications.
  • Superior Sensor Technology was established with the objective to revolutionize the high performance, cost driven pressure sensor market by developing integrative, highly intelligent solutions for industrial, HVAC and medical applications.

2 Day Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers Course - September 8-9, 2021 - ResearchAndMarkets.com

Monday, June 14, 2021 - 10:53am

The "Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers" training has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers" training has been added to ResearchAndMarkets.com's offering.
  • This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environmental Monitoring Program requirements, Excursion investigations, DataTrending, Microbiological processes/methodology, Cleanroom cleaning/disinfection.
  • The types of micro-organisms, typical mitigation steps in ensuring an effective contamination control through Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures),Gowning Controls, Personnel Training, Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy), Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program and the Basics of Sterilization Processes- Physical and Chemical Processes will also be discussed.
  • The various regulatory bodies' requirements such as 21 CFR Part 211 (mostly relevant 211.113 "Control of microbiological contamination", ISO 14644 (Various Parts), FDA Guidance for Industry: Sterile Drug Products Produced By Aseptic Processing - Current Good Manufacturing Practice") amongst others and the criticality of aseptic processing and other key contamination control evaluators during the manufacture and testing of products are important to the quality determination and release of the finished manufactured products.