-
Dec 6, 2024 | 
bioprocessonline.com | Kishore Kumar Hotha |Michael Moussourakis |Jeff Phillips |Stacy Silverstein
Let Us Handle Your Buffer PreparationThermo Fisher Scientific is here to support you with the buffer preparation in your manufacturing workflow. Leaving the non-core activities to us enables you to focus on the patient therapy development. Our capabilities cover off-the-shelf products like WFI, NaOH, NaCl, or EtOH, a library of the most frequently used buffers that are made-to-order, as well as fully customized buffers.
-
Sep 11, 2024 | 
skyandtelescope.org | Jeff Phillips
The Essential Guide to AstronomyMENUThe Essential Guide to Astronomy<< Back to galleryPhotographer:Jeff PhillipsLocation of Photo:Eugene, OregonDate/Time of photo:September 09, 2024 8:05.2 UTEquipment:C14 at f/20 with ZWO 224 color cameraDescription:See was above average, 4/5 on the Clear Sky Chart scale. I was able to see the curve of the Cassini division on the live view at least some of the time. I shot 9 five minute videos of Saturn, the best four results were combined with Winjupos.
-
Sep 6, 2024 | 
bioprocessonline.com | Matthew Pillar |Todd Andrews |Michael Moussourakis |Jeff Phillips
FOCUS ON FACILITIES DESIGNThe wave of ADC (antibody-drug conjugate) development and manufacturing activity we’re currently witnessing, and importantly, the HPC (high-potency compounds) comprising the payloads in these therapies, demand thorough assessment of development and manufacturing facility design. Single-Use vs.
-
Aug 13, 2024 | 
meddeviceonline.com | Yadnyesh Patel |Michael Moussourakis |Jeff Phillips |Stacy Silverstein
Join us at The MedTech Conference in Toronto from October 15-17. Connect with industry leaders, explore cutting-edge innovations, and help shape the future of health care. Experience the revamped Medtech Campus, hands-on tech showcases, interactive sessions, and unparalleled networking opportunities. Don't miss this chance to be part of the pivotal event in the medtech industry.
-
Aug 9, 2024 | 
jdsupra.com | Jeff Phillips
Unstructured Data Cleanup is an information governance practice focused on the permanent deletion of information that is no longer of use to the business. Using a scanning and classification tool, organizations can better understand the information they manage and determine if it can be defensively disposed, or if there is a regulatory, legal, or business reason why it must be retained.
-
Aug 9, 2024 | 
bioprocessonline.com | Matthew Pillar |Michael Moussourakis |Jeff Phillips |Stacy Silverstein
AI and machine learning are the buzzwords of the decade, often accompanied by lofty promises — but what do they really mean for biopharma? How can these technologies be adopted to improve biomanufacturing processes, testing, and quality? Join Bioprocess Online Live for an exploration into the practical applications of AI/ML in biomanufacturing, its barriers to adoption, and how regulators can help standardize use across the industry. Registration is free thanks to the support of Atum Bio.
-
Jul 9, 2024 | 
meddeviceonline.com | Jayet Moon |Arun Mathew |Jessica Sanford |Jeff Phillips
Get the latest industry news and expert insights delivered straight to your inbox!
Newsletter
| July 9, 2024
The waterfall model and the V-model are commonly employed in medical device development. In our new era of the Quality Management System Regulation (QMSR), risk management can be integrated with the design control process. RFID For Med Devices: Identifying A PartnerRFID is increasingly being used in medical devices.
-
May 30, 2024 | 
mondaq.com | Jeff Phillips
Unstructured Data Cleanup is an information governance
practice focused on the permanent deletion of information that is
no longer of use to the business. Using a scanning and
classification tool, organizations can better understand the
information they manage and determine if it can be defensively
disposed, or if there is a regulatory, legal, or business reason
why it must be retained.
-
May 17, 2024 | 
bioprocessonline.com | Erich Bozenhardt |Michael Moussourakis |Jeff Phillips |Stacy Silverstein
FOCUS ON FACILITIES DESIGNAfter decades of helping to rescue biotech and pharma companies from environmental monitoring excursions, Herman and Erich Bozenhardt bring this discussion about specific problems you should avoid. Steps For Proper Cleaning ValidationExamine the steps of cleaning validation for both low-volume and high-volume manufacturers and the important role these studies play.
-
May 16, 2024 | 
meddeviceonline.com | Erika Roberts |Michael Moussourakis |Jeff Phillips |Stacy Silverstein
Get the latest industry news and expert insights delivered straight to your inbox!
Newsletter
| May 16, 2024
The FDA recently announced that they have seen an increase in the number of entities that contract out testing or services where the data provided by said firms was fabricated, duplicated, or just deemed “unreliable.” Here's what you can do.
