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Top Stories
The acquisition will boost Merck's pipeline for cancer, fibrosis, and autoimmune disease therapeutics.
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The US Federal Trade Commission (FTC) has requested additional information from Roche and Spark Therapeutics regarding Roche's pending $4.3-billion acquisition of Spark.
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Industry News
The Michelson Medical Research Foundation and the Human Vaccines Project have awarded three young scientists $150,000 for their novel approaches toward human immune system research.
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ABPI has published a guide for pharmaceutical companies on how to work successfully, collaboratively, and ethically with patients and patient groups, in line with the ABPI Code of Practice.
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Biopharma News
In this collaboration, AbCellera will apply its expertise to generate panels of antibody candidates for Gilead to evaluate.
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GSK has revealed that it has entered into a five-year collaboration with the University of California to advance genomic research and improve drug discovery.
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Supplier News
The acquisitions, totaling $50 million, are expected expand Aptar Pharma's service offerings to support complex product development.
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Dassault Systèmes, a provider of virtual universes to imagine sustainable innovations, has signed a definitive agreement to acquire Medidata Solutions in an all-cash transaction.
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Regulatory News
Vida International received an FDA warning letter after an inspection found quality control violations.
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The two countries have been included into the mutual recognition agreement between the European Union and the US FDA that recognizes facility inspections conducted in different territories.
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FEATURED TOPICS |
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DRUG DELIVERY
Research advances have enabled the application of nanotechnology to drug delivery. What does this technology offer in the way of enhancing therapeutic effect?
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SUPPLY CHAIN/LOGISTICS
Proactive approaches that consider long-term supply chain security compliance are recommended to ensure companies stay on the right track.
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REGULATORY/GMP COMPLIANCE
Stuart Jones, regulatory quality assurance professional in good laboratory practice (RQAP-GLP) and director of quality assurance at PPD Laboratories' Bioanalytical Laboratory shared GLP best practices with BioPharm International.
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June 25–26, 2019
September 3–4, 2019
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Experts share insight and advice for conducting CMC due diligence with contract development organizations, using multiple attributes methods to monitor quality attributes, and strategies for using specialized services for biopharmaceutical development applications.
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