June 11th 2024
Swiss CDMO CordenPharma and Spain-based Certest will collaborate on the development of ionizable lipids for LNP formulations.
May 21st 2024
The need for preclinical testing expertise is growing as molecular complexity increases.
May 4th 2024
A comparison between polysorbates and HPβCD determines the better stabilizer for biologics formulation.
September 13th 2023
Despite the successes that have already been achieved with emerging therapy development and manufacturing, companies are still facing numerous challenges.
August 23rd 2023
WuXi XDC will provide end-to-end services to support Boostimmune’s discovery of novel bioconjugates.
Keeping it Simple: Collaborating for Success in Drug Delivery
For successful drug delivery partnerships, it’s important to take a long-term view, focus on simple designs, and address potential payer concerns up front.
Althea Patents Method to Crystallize Proteins
The company’s method reduces the time required to crystallize antibodies from weeks to one day.
Intertek Explores the Reformulation of Intravenous Biologics
The company plans to reformulate injectable products to make them into inhaled and intranasal medications.
Catalent Expands Biologics Capabilities
Expansions at Catalent’s Kansas City, MO, and Madison, WI facilities made in response to industry demand.
Catalent Adds Platform for Antibody Combination Therapies
Catalent’s licensing of Excelimmune’s antibody combination therapy platform can enable more consistent, cost effective production of antibody combinations.
Capsugel Completes New Spray-Dried Dispersion Manufacturing Facility
The new facility expands the company’s commercial manufacturing capability at its Bend, Ore. site.
Taking a “Development-by-Design” Approach to Cell Therapies
Whether outsourcing or developing cell therapies in-house, success demands a focus on quality, cost of goods, and sustainability from the start.
CPhI Pharma Insights: Formulation and Ingredients Report
The report highlights a need for greater third party certification to ensure GMP vigilance.
EMD Millipore Opens New R&D Center
The facility, which includes state-of-the-art formulation, analytical and synthetic laboratories as well as a customer training center, will focus on bioavailability enhancement and oral dosage formulations.
Trends and Challenges in Biologics Outsourcing: A Q&A with Stephen Taylor
Stephen Taylor PhD, vice-president and commercial director at Fujifilm Diosynth Biotechnologies, addresses some of the challenges facing biologics outsourcing.
Contract Services Spending: Who's Spending What, and Where?
A survey provides insight into drug companies' plans for spending on outsourced services. This article contains bonus online material.