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Daiichi Sankyo, Inc.Daiichi Sankyo Pharma Development is the product development arm of the U.S. organization, engaged in Clinical Development, Translational Medicine & Clinical Pharmacology, Regulatory Affairs & Risk Management, Informatics & Knowledge Management, Biostatistics and Data Operations and Development Research. We conduct clinical studies and expedite product registrations for the United States and Europe, and collaborate with our Tokyo parent company on all of our global product development projects as well.We are led by a group of highly experienced pharmaceutical executives who have gained broad experience at some of the world's leading pharmaceutical companies. In addition, we have a.significant number of senior staff from Japan to assist in and coordinate our global development activities. Along with our staff of about 200 employees, we utilize outsourcing strategies for.additional functional support. One such example is our partnership with MDS Pharma Services to establish the company's first collaborative clinical pharmacology unit. The unit is located in New Jersey and focuses on the evaluation of novel treatments for diabetes and lipid disorders. Daiichi Sankyo, Inc. has just completed the integration of its two legacy companies that resulted in a new R&D organization -- including new processes and improved decision-making systems aimed at speeding global development.
| Contact Details: |
| Two Hilton Court |
| Parsippany |
| New Jersey |
| 07054 |
| United States of America |
| Tel: | 973 359 2600 |
| Fax: | 973 359 2645 |
| Email: | smallbusinessplan@daiichisankyo-us.com |
| WWW: | www.sankyo-pharma.com/

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Press Releases on Daiichi Sankyo, Inc.:
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| New Updates to AHA/ACC/SCAI Clinical Guidelines Recommend Treatment with Effient(R) for Patients with Acute Coronary Syndromes Managed with PCI |
18th November, 2009 |
Eli Lilly and Company |
PARSIPPANY, N.J. and INDIANAPOLIS, Nov. 18 /PRNewswire-FirstCall/ -- Effient® (prasugrel) tablets, a new antiplatelet medicine, was added as a treatment option in two clinical guideline updates: one
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| Effient(R) Exhibited Greater Antiplatelet Activity than High Dose Clopidogrel in Type 2 Diabetes Mellitus Patients with Coronary Artery Disease |
15th November, 2009 |
Eli Lilly and Company |
ORLANDO, Fla., Nov. 15 /PRNewswire-FirstCall/ -- Results from a new study showed patients with type 2 diabetes mellitus who also had coronary artery disease (CAD) and received a 60 mg loading dose and
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| Welchol(R) (colesevelam HCl) Receives FDA Approval to Lower LDL Cholesterol in Pediatric Patients with Heterozygous Familial Hypercholesterolemia |
7th October, 2009 |
Daiichi Sankyo, Inc. |
-- improve glycemic control in adults with type 2 diabetes mellitus
Important Limitations of Use
-- Welchol should not be used for the treatment of type 1 diabetes or for
the
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| Survivors of Heart Events: What Does it Take to Get Back to Living? |
22nd September, 2009 |
Eli Lilly and Company |
-- 93% of patients who feel they had been given a second chance in life
viewed it as an opportunity to do things better.
-- Only 17% strongly agreed that they were worried about
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| Daiichi Sankyo and Lilly Receive U.S. FDA Approval for Effient(TM) |
10th July, 2009 |
Eli Lilly and Company |
PARSIPPANY, N.J. and INDIANAPOLIS, July 10 /PRNewswire-FirstCall/ -- Daiichi Sankyo, Inc. and Eli Lilly and Company (NYSE: LLY) today announced that the U.S. Food and Drug Administration (FDA)
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