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Merck Announces U.S. FDA Filing Acceptance of New Drug Application (NDA) for MK-1293, an Investigational Follow-On Biologic Insulin Glargine

2016-08-05 14:00:00| Merck.com - Research & Development News

Dateline City: KENILWORTH, N.J. Marketing Authorization Application to the European Medicines Agency Currently Under Review KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside of the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the New Drug Application (NDA) for MK-1293, an investigational follow-on biologic1 insulin glargine candidate for the treatment of people with type 1 and type 2 diabetes, which is being developed by Merck with partial funding from Samsung Bioepis. Language: English Contact: MerckMedia:Doris Li, 908-246-5701orKristen Drake, 908-236-4223orInvestors:Amy Klug, 908-740-1898 Ticker Slug: Ticker: MRK Exchange: NYSE read more

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US Navy's future littoral combat ship USS Detroit completes acceptance trial

2016-07-25 01:00:00| Naval Technology

The US Navy's Freedon-class variant USS Detroit littoral combat ship (LCS 7) has successfully completed acceptance trial, prior to future deployment.

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Factory and Acceptance Test Engineer for Ground Stations

2016-07-21 18:07:02| Space-careers.com Jobs RSS

LSE Space GmbH is looking for an experienced Engineer mf in order to fulfill the task of Factory and Aceptance Test Engineer for Ground Stations at our customer ESAESOC in DarmstadtGermany. The primary responsibilities of this role will be Support to project development, in terms of definition of technical specifications and statement of work, participation for design review as well as participation to factory and site acceptance tests. Participation in the definition, execution and evaluation of predevelopment studies by Industrial Contractors, related to frequency and timing systems. Support in the definition of requirements for frequency and timing systems, and participation in preliminary prototype and bread boarding activities. Monitoring and critical evaluation of activities related to frequency and timing systems development by Industrial Contractors. Engineering maintenance and enhancement of frequency and timing systems. Monitoring under ESA responsibility of developmentprocurement activities contracted to external industries this includes engineering analysis, participation to reviews and meetings, participation to Factory and Site Acceptance Tests, etc. Engineering support to corrective maintenance task, for problem requiring specific technical background in frequency and timing systems. Engineering support to ESTRACK preventive maintenance tasks Engineering support to operations. Qualifications and skills University degree Experience in Design and procurement of frequency and timing systems Caesium and rubidium based frequency and timing systems in 15m. antennas Maser based frequency and timing systems mainly in 35 m. antennas Optical clocks Microwave Sapphire clocks Optical fibre clock distribution Benefits A permanent employment contract. Competitive salary plus a comprehensive benefits package. Career path. Security In line with Asylum Immigration Legislation, all applicants must be eligible to live and work in the EU. Documented evidence of eligibility will be required from candidates as part of the recruitment process. Furthermore, in view of the nature of the work the company is in, all potential employees will undergo stringent reference and identity checks. You are looking for a challenging position in a very interesting, international environment? Then send your application preferably online to not later than 26th August 2016 Daniel Gestal daniel.gestallsespace.com

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US Navys future expeditionary fast transport vessel Carson City completes acceptance trials

2016-06-08 01:00:00| Naval Technology

The US Navy's newest expeditionary fast transport (EPF) vessel, the future USNS Carson City (EPF 7), has completed acceptance trials during an underway period in the Gulf of Mexico.

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H3 Biomedicine Receives FDA Acceptance For Investigational New Drug Application

2016-06-01 06:06:14| drugdiscoveryonline Home Page

H3 Biomedicine Inc., a biopharmaceutical company specializing in the discovery and development of precision medicines for oncology and a member of the Eisai Group, announced recently that the U.S. Food and Drug Administration (FDA) accepted the company’s Investigational New Drug (IND) application to begin Phase 1 clinical trials for its lead oncology drug candidate H3B-8800

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