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FDA rejects Amphastar’s nasal opioid overdose treatment

Feb 22, 2017
Amphastar Pharmaceuticals Inc said on Tuesday that the U.S. Food and Drug Administration had rejected its application to market an intranasal version of the emergency opioid-overdose…
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Valeant Pharmaceuticals and EyeGate Enter into Licensing Agreement for EGP-437 Combination Product

Feb 22, 2017
Valeant Pharmaceuticals International, Inc. and EyeGate Pharmaceuticals, Inc., a specialty pharmaceutical company that focuses on developing and commercializing products for treating…
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Abzena signs antibody manufacturing development deal with University College London

Feb 22, 2017
Abzena has entered into a manufacturing agreement with University College London (UCL). Under the agreement, Abzena will manufacture Magacizumab, an antibody created using the…
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Xbrane Biopharma obtains GMP certification for Spherotide production facility

Feb 21, 2017
Xbrane Biopharma has been granted GMP (Good Manufacturing Practice) certification for its Spherotide production facility by AIFA, the Italian Medicines Agency. The GMP certification…
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ICON Selected by the FDA to Validate Patient-Reported Outcome Endpoints for Antibacterial Drug…

Feb 21, 2017
ICON plc, a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries, today announced that it has been awarded a…
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CTT Pharmaceutical Holdings and CanniMed Therapeutics Inc. Complete Exclusive Canadian Licensing…

Feb 20, 2017
CanniMed Therapeutics Inc. and CTT Pharmaceutical Holdings Inc.have entered into a definitive contractual relationship for the licensing of CTT’s Orally Dissolvable Thin Film (ODF)…
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Immune Pharmaceuticals Announces the launch of REMAIN

Feb 20, 2017
Immune Pharmaceuticals Inc., will announce on Monday, February 20th, 2017 at the Acute Leukemia XVI symposium in Munich, Germany that it will be launching REMAIN™, an international…
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FDA accepts Intellipharmaceutics’ NDA for Rexista to treat moderate to severe pain

Feb 20, 2017
The US Food and Drug Administration has accepted for filing of Intellipharmaceutics International’s New Drug Application ("NDA") seeking authorization to market its Rexista…
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Momenta announces FDA warning letter to contracted Glatopa’s fill/finish manufacturer

Feb 20, 2017
Momenta Pharmaceuticals has announced that Pfizer, Sandoz’s contracted Glatopa (glatiramer acetate injection) fill/finish manufacturing partner has received a warning letter from the…
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Arix Bioscience raises £100m in IPO

Feb 20, 2017
Global healthcare and life science company Arix Bioscience has raised £100m in its Initial Public Offering (IPO) on the main market of the London Stock Exchange. The Offer was…
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Press Releases

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