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February 10, 2010
PPD’s global central lab operations in Singapore has earned accreditation by the College of American Pathologists (CAP), validating its ability to deliver high-quality, reliable data that meet excellence standards designed to enhance patient safety
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February 9, 2010
Azopharma Drug Development Services has received approval from the Medicines and Healthcare products Regulatory Agency (MHRA) for production of commercial product.
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February 8, 2010
Teva Pharmaceutical Industries, Ltd. and Active Biotech have amended their marketing and distribution agreement for oral laquinimod, an investigational drug for relapsing-remitting multiple sclerosis (RRMS).
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February 5, 2010
Analytical Bio-Chemistry Laboratories (ABC) has expanded its capabilities to include comprehensive support for large molecule development.
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February 5, 2010
Gorbec Pharmaceutical Services is opening a GMP-compliant analytical lab in Yantai, China.
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February 2, 2010
Dalton Pharma Services has successfully completed its Health Canada audit and has received a 'compliant' rating for its GMP manufacturing facility.
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February 1, 2010
Catalent Pharma Solutions has expanded its capabilities to include a new potent products area at its Schorndorf site in Germany.
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February 1, 2010
Cephalon, Inc. has signed an agreement to acquire Mepha AG and its subsidiaries for $590 million.
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January 29, 2010
Regis Technologies, Inc. received an Establishment Inspection Report (EIR) from the FDA stating that the company has passed pre-approval inspection (PAI) for the manufacture of 4-Aminopyridine, the active ingredient in Ampyra.
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January 25, 2010
Sinobiopharma’s production facility for solid dosage Perindopril has passed Chinese State Food and Drug Administration (SFDA) inspection and is now approved for production and marketing.
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January 21, 2010
Patheon began construction of a new pharmaceutical development center at its existing manufacturing facility in Bourgoin-Jallieu, France.
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January 21, 2010
AlphaRx Inc.’s licensee, Gaia BioPharma Ltd., has signed an agreement with a CMO to manufacture GAI-122 for use in Phase I and II trials.
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January 21, 2010
NextPharma Technologies’ expansion of its Cold Chain and Logistics (CLS) business in Austria has received full regulatory approval and has been granted a Distributors-Manufacturers License by the Austrian Federal Office for Safety in Healthcare.
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January 20, 2010
Ricerca Biosciences has validated and implemented Watson Laboratory Information Management System (LIMS) for its bioanalysis division.
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January 19, 2010
AMRI has received certification of its high potency research labs and GMP-manufacturing facilities in Rensselaer, NY for the safe handling of potent APIs by SafeBridge Consultants, Inc.
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