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March 17, 2011
The Bulk Pharmaceutical Task Force (BPTF) of the Society for Chemical Manufacturers and Affiliates (SOCMA) and the European Fine Chemicals Group (EFCG) of the European Chemical Industry Council (CEFIC) are calling on FDA to mandate inspections of foreign active pharmaceutical ingredient (API) manufacturing sites with the cost borne by those sites being inspected. Both organizations have indicated a willingness to pay fees for these inspections when performed on their member-owned facilities that are located outside the United States.
March 03, 2011
Fujifilm and Merck & Co. have formed a definitive agreement by which Fujifilm will acquire the Merck BioManufacturing Network, a contract biopharmaceutical manufacturing and development business of Merck.
Pfizer Completes King Acquisition; ViiV Healthcare Names Chairman; and More.
March 02, 2011
Brazil develops its first national plasma fractionation plant.
Q&A with Robert Hardy, chief executive of Aesica
The power of emerging markets is reflected in the pharma's sales and production positions.
INTERPHEX 2011 aims to address the industry's unique characteristics.
The authors outline the key decision points FDA must consider in putting forth a US regulatory pathway for biosimilars.
This article is Part I of a three-part series on biopharmaceutical issues in public health, government, and developing-world markets. Part 1 focuses on drug-development. Part II, which examines manufacturing, appeared in the April 2011 of Sourcing and Management. Part III, which analyzes distribution and administration,appeared in the May 2011 issue.
Contract manufacturers and fine-chemical suppliers announce capacity expansions and service enhancements of Informex.