Matica Biotechnology, Inc. (Matica Bio), a contract development and manufacturing organization (CDMO) specializing in the clinical and commercial production of cell and gene therapies, ceremonially broke ground today on its new 25,000 ft2 facility which will house its GMP virus production suites, development laboratories and company offices. The new building will be located in Providence Park at 2501 Earl Rudder Freeway in College Station.
Cleanroom Design Build Articles
SkyWater Announces MOU to Provide Domestic Advanced Packaging Capabilities as Reshoring Momentum Builds for Semiconductor Supply Chain
SkyWater Technology, the trusted technology realization partner, today announced it has entered into an exclusive, non-binding Memorandum of Understanding (MOU) with Osceola County, Florida to explore taking over the lease of the Center for Neovation, a state-of-the-art 200 mm semiconductor manufacturing facility, by forming a new public-private partnership for microelectronics manufacturing and advanced packaging capabilities. Following the MOU, SkyWater, the only U.S
Sorrel Medical Opens New Manufacturing Cleanroom Facility
Sorrel Medical, a developer and manufacturer of wearable drug delivery devices, today announced the opening of a new manufacturing facility with state-of-the-art cleanroom facilities to accommodate manufacturing scalability of its wearable drug delivery devices.
ACROMEC Healthcare Pharma Cleanroom Contract Worth $6.2M
ACROMEC Limited (“ACROMEC”, SGX:43F), an established specialist engineering service provider in the field of controlled environments serving mainly the healthcare, biomedical, research and academia sectors, has secured three new contracts totaling approximately S6.2 million.
Cleanroom Technology Awards
The winners of the Cleanroom Technology Awards 2018 have been announced. The awards have been introduced to recognize and reward achievements, celebrating the best product innovations from those exhibiting at the Cleanroom Technology Conference 2018.
Life Sciences Cleanroom Manufacturing Facility
Ecolab Inc., the global leader in water, hygiene and energy technologies and services, continues to expand its Greensboro campus with construction of a life sciences cleanroom manufacturing facility to support the launch of the company’s Life Sciences solution portfolio in North America.
Single Pass Versus Recirculating Clean Rooms
The decision that will influence the design of a cleanroom air handling system determining the method to use should be made depending of the desired preciseness of your control. If you are controlling temperature and humidity very tightly, you want to use a recirculating system so that once you’ve conditioned that air, you are not letting the conditioned air escape.
Micron to add new nanofab production cleanroom
Semiconductor giant Micron Technology broke ground in North Coast yesterday to add new cleanroom space for production of its 3D NAND flash memory products. Micron did not disclose the cost, except to say that the new facility will be a “multi-billion- dollar investment”. It will be equipped over the next five years or more and add 1,000 new jobs in Singapore. As part of its agreement with the Economic Development Board, Micron will also broaden its research and development (R&D) capabilities here. The 1,000 new roles it is adding will comprise mainly engineers and technicians related to R&D and manufacturing.
HVAC and GMP Environment Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Cleanroom HVAC Design
Standards and Classifications, Particle/Contamination Sources and Control, Design Considerations, Flow Patterns and Floor Arrangements, Airflow Quantity and Demand Flow Control, Pressurization and Airlocks, in addition to Typical HVAC Air-Handling Systems and Selection.
ISO Cleanroom Standards Committee
ISO cleanroom standards offer international consistency and have been developed by a technical committee of controlled environment subject matter experts.
Clean Room Windows Selection
What factors should you consider when evaluating clean room windows? When does provide visibility into a clean room operation without allowing people into the clean room operation. This promotes a cleanly environment and decreases the possibility of contamination.
The most important part of maintaining a clean environment as it corresponds to clean room windows, you want to ensure that there are minimal window ledges in the clean room environment. Ledges are a great place to collect contaminants that could set back your queen room operation.