Archive for the ‘Facilities’ Category

An API Regulations Update from the ICH Q3D Metal Impurities Workshop

Friday, April 20th, 2012

As SAFC Live previously reported, the  ICH Q3D Metal Impurities Workshop was held from April 4-5, 2012 at the Marriott Bethesda North Hotel in Bethesda, Maryland. The program focused on the new limits for element impurities in drug products and how they may impact businesses in the pharma industry. On day one, SAFC Quality Assurance Director, Patty Benson, participated in a panel titled “Perspectives From Active Pharmaceutical Ingredient (API) Suppliers”, along with a lineup of speakers from industry colleagues, the IPEC-Americas, CHPA and SOCMA’s Bulk Pharmaceutical Task Force (BPTF). The panel talked about draft guidelines and data implications, and their impact on pharmaceuticals. Patty’s input from an API maker’s perspective was complemented with an excipient user perspective from Janeen Skutnik-Wilkinson, Director of Quality and Regulatory Policy at Pfizer Inc. and an excipient maker perspective from David Schoneker, Director of Global Regulatory Affairs at Colorcon.

Patty’s presentation in the “Perspectives From Active Pharmaceutical Ingredient (API) Suppliers” panel is available for reference here: Q3D BPTF 0412.

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SAFC Lives: Toru Kobayashi, SAFC Manager in Tokyo, Japan

Friday, March 23rd, 2012

Toru Kobayashi, SAFC Manager, Tokyo

Recently, SAFC Live caught up with Toru Kobayashi, SAFC Manager in Tokyo, Japan at CPhI Japan, where he gave us an overview of the Japanese market and shared an award that SAFC received for ten years of participation at CPhI Japan. Here, we had an opportunity to speak with Toru on a more personal level in this next installment of SAFC Lives.

SAFC Lives presents personnel profiles where we talk to the people and personalities who make SAFC tick, and find out something about their work, what drives them, their aspirations, and what they enjoy doing when they’re not playing a critical role in the ongoing growth of SAFC.

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An In-Depth Interview with SafeBridge President and CEO, John Farris

Friday, November 4th, 2011

SAFC’s Verona plant has just been awarded SafeBridge Certification. But what does this mean, and what does the process involve? SafeBridge President and Chief Executive, John Farris, tells all in the following interview with SAFC Live.

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Optimizing High-Potency Manufacturing – An industry snapshot by PharmaTech’s Patricia van Arnum

Tuesday, June 7th, 2011

Great article by Patricia van Arnum in the latest issue of Pharmaceutical Technology that talks about the importance of effective containment measures in API manufacturing and how a variety of process, equipment, and operational considerations need to be taken into account.  From facility design to handling and storage procedures to the processes used in manufacturing to the choice of equipment deployed, specialist knowledge and approaches are necessary to ensure that containment and minimal exposure of employees is achieved.

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CPhI Focus: in-Pharma Technologist speaks with Gilles Cottier and Mark Cassidy

Thursday, October 14th, 2010

It was all hands to the pump last week in Paris as SAFC embarked upon a packed media schedule during CPhI.  SAFC President Gilles Cottier and Mark Cassidy, President and VP of contract manufacturing services, were on hand to talk with in-Pharma Technologist’s Gareth MacDonald about the recent completion of the expansion of the company’s manufacturing plant in Jerusalem, Israel, further increasing its global footprint.

“In this exclusive video interview, Cottier and Cassidy told in-Pharmatechnologist that growing industry demand for high potency active pharmaceutical ingredients (APIs) was the key driver for the investment. Cottier also explained that the addition of such capability is an important part of differentiating SAFC’s offering in the increasingly competitive global contract manufacturing sector. The 50,000 expansion includes capacity for bulk drugs, secondary metabolites, cytotoxins and a range of large molecules proteins.”

Watch the whole interview here.

CPhI News… SAFC Completes Expansion of High-Potency Fermentation Capabilities at Israel Site

Wednesday, October 6th, 2010

SAFC today announced the completion of a state-of-the-art expansion of its Jerusalem, Israel facility. The additional capacity expands SAFC’s contract manufacturing capabilities in large molecule recombinant proteins and small molecule Active Pharmaceutical Ingredients (APIs) through fermentation, including High Potent APIs (HPAPIs) and secondary metabolites.

The 50,000 sq. ft. cGMP fermentation expansion, which is expected to begin production later in October 2010, will focus on niche fermentation of APIs and bulk drugs, producing secondary metabolites (antibiotic-like molecules), cytotoxins and large-molecule proteins. A 30,000 sq. ft. area of the new facility has been designed to be Biosafety Level 2 compliant – enabling manipulation of human pathogens. Capabilities include 1,000 and 4,000-liter tank capacities for bacterial and fungal fermentation, as well as explosion-proof suites.

“Fermentation is a long-standing technology, yet new applications have been recently discovered, including the synthesis of high potency compounds, which is a major growth area currently driving contract manufacturers such as SAFC to look beyond traditional active pharmaceutical ingredient (APIs),” said SAFC President, Gilles Cottier. “The Jerusalem expansion builds upon over 30 years of Sigma-Aldrich experience in the development and manufacture of hundreds of microbial-derived products, and is expected to help SAFC augment its industry-leading strategy of strength and expertise in emerging, highly-specialized technologies and difficult to manufacture products.”

At the Jerusalem facility, SAFC employs E.coli, Streptomyces sp., filamentous fungi and yeast, including risk group 2 human pathogens, across a wide product portfolio that includes small organic molecules and peptides, as well as larger molecules such as proteins, lipids and carbohydrates or macromolecules.

“We believe a primary differentiator at our Jerusalem site is our capability to safely manufacture niche small molecule products and biologics such as natural or recombinant proteins,” added Cottier. “In addition to having industry-leading techniques, capability and infrastructure to manufacture fermentation derived HPAPIs, the site is a multi-disciplinary, full-service facility offering purification and analytical expertise associated with fermentation technology such as microbiology, organic chemistry, biochemistry and molecular biology.”

Pharma magazine talks about SAFC’s HPAPI expansion plans….

Monday, September 27th, 2010

Corrine Lawrence, Editor of Pharma magazine, recently spoke with SAFC about the company’s aggressive expansion program that is bolstering manufacturing capabilities in the high potency API space.  The recent addition of a cGMP-validated extension to SAFC’s Madison, Wisconsin plant is just the latest in a series of investments made by the company in high potency manufacturing in the past couple of years.  Reflecting the demand being seen from customers, who require ever-growing amounts of high potency compounds in order to manufacture the growing number of high-efficacy, targeted therapeutics being brought to market, SAFC has a program of ‘centers of excellence’ and is investing to match the needs of customers.

You can read the full Pharma article here