Miriam Guest

Feb 16, 2023 | biosimilardevelopment.com | Tim Sandle |Miriam Guest |Lisa Cherry

By Miriam Guest, principal microbiologist, AstraZeneca Confirmation of microbial quality of drug products manufactured by CDMOs is a key component of product release. It is important to ensure that laboratory-specific method suitability testing is performed to ensure appropriate recovery of the presence of potential contaminants.

Feb 15, 2023 | outsourcedpharma.com | Louis Garguilo |Miriam Guest |Alok Tayi

By Louis Garguilo, Chief Editor, Outsourced Pharma If cell therapy is the art of engineering, the  of these therapies – many of which are stymied by an inability to scale up or produce at various locations  –is fully contingent upon the application of engineering concepts and practices. Part two of our look into "cell therapy industrialization."

Feb 15, 2023 | outsourcedpharma.com | Louis Garguilo |Miriam Guest |Alok Tayi

By Louis Garguilo, Chief Editor, Outsourced Pharma If cell therapy is the art of engineering, the  of these therapies – many of which are stymied by an inability to scale up or produce at various locations  –is fully contingent upon the application of engineering concepts and practices. Part two of our look into "cell therapy industrialization."

Feb 15, 2023 | outsourcedpharma.com | Miriam Guest |Alok Tayi |Louis Garguilo

By Miriam Guest, AstraZeneca In microbial enumeration testing, the product-specific interferences are addressed during method development. The execution can vary between laboratories. This article examines general considerations, membrane filtration, and the pour plate method. By Each month, works in conjunction with PharmSource, part of GlobalData, to present its “Contract Manufacturing: Opportunities and Threats (CMOT) Report” to our readers.

Feb 3, 2023 | pharmaceuticalonline.com | Miriam Guest |Yiming Ma |Martín González

By Miriam Guest, principal microbiologist, AstraZeneca Confirmation of microbial quality of drug products manufactured by CDMOs is a key component of product release. It is important to ensure that laboratory-specific method suitability testing is performed to ensure appropriate recovery of the presence of potential contaminants.