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March 17, 2022

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Selecting In-Vitro Dissolution Methodologies For Amorphous Solid Dispersions

Many novel drug candidates aimed at addressing unmet medical needs are OSDs classified as poorly soluble, calling for formulation strategies that can increase bioavailability. In vitro dissolution testing can help assess bioperformance, but only if the most appropriate testing methods are selected.

	Industry News

BioMed X Institute and Merck KGaA, Darmstadt, Germany, Start Second Research Project in Immunology
A German independent research institute, BioMed X, announced the start of its new research project ‘... read more »

AbbVie and Scripps Research Announce Collaboration to Develop Antiviral Treatments for COVID-19
AbbVie and Scripps Research announced a global collaboration to develop potential novel, direct-... read more »

AstraZeneca Update on Regulatory Review of Fasenra in Chronic Rhinosinusitis with Nasal Polyps
The FDA has issued a complete response letter (CRL) regarding the supplemental Biologics License ... read more »

Lynparza Approved in US as Adjuvant Treatment for Patients with Germline BRCA-Mutated HER2-Negative High-Risk Early Breast Cancer
AstraZeneca and MSD’s Lynparza (olaparib) has been approved in the US for the adjuvant treatment of ... read more »

	Infographic

Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Recombinant Horseshoe Crab Factor C (rFC) provides a sustainable, highly effective, and environmentally friendly sustainable means of endotoxin ... read more »

	Featured Articles

Validation Strategy for New Recombinant Factor C Users This paper presents Roche’s validation strategy of the recombinant factor C (rFC) endotoxin testing method. The validation approach uses statistical ... read more »

Enabling Technologies Consortium: Implementations of Wearable Enhanced Knowledge and Analytics Platforms for Pharmaceutical Laboratories Core tools used for research and development in pharmaceutical laboratories, such as media capture, integration, and electronic notebooks, have not ... read more »

	Featured Video

On-Demand Webinar: Viral Control in Pharmaceutical Processing
This webinar discusses the essential elements of control, testing, and remediation and it includes a spotlight on the maim viruses of concern. watch »

On-Demand Webinar: In-situ Forming Extended Release Injectable Depot Systems from Lactide / Glycolide Chemistry
This webinar will provide scientists and technical stakeholders working in drug delivery with a detailed explanation of theory and application of an ... watch »

	Featured Products

Luminata Product Development Software
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	Featured Whitepaper

Whitepaper: Key Considerations for Extracting Proteins from Recombinant Host Cells
In the biopharmaceutical industry, quality is pivotal. For a final product to meet quality standards, quality must be built into the production process. Biopharmaceuticals, however, are made from ... read more »

Whitepaper: QC Executive Q&A - Research and Development of Protein-Based Therapeutics
As a global provider, MilliporeSigma offers a wide range of products and services to biopharma. On the analytical side, we have a growing selection of chromatography and sample preparation products ... read more »

	Events

SMi’s 9th Annual Conference Pre-Filled Syringes East Coast
Boston, MA – 04/25/2022
The global pre-filled syringes market was valued at $1139.6 million in 2020 and with the rapid growth of the industry, is expected to grow at a CAGR ... event details »

IFPAC 2022
North Bethesda, MD – 06/12/2022
IFPAC brings together experienced professionals and the next generation of leaders to share in discussions, give input and get ideas for the future ... event details »

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