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Intersect ENT Receives CE Mark Approval for PROPEL ...

Intersect ENT Receives CE Mark Approval for PROPEL ...

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 · Intersect ENT Receives CE Mark Approval for PROPEL® Contour for Patients with Chronic Rhinosinusitis Following Frontal Sinus Surgery. .

Novartis prostate cancer drug receives FDA ...

Novartis prostate cancer drug receives FDA ...

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 · Novartis, which acquired the therapy with its billion purchase of Endocyte three years ago, has a growing portfolio of radioligand medicines that includes already approved cancer therapy ...

Telit News Center: Recent Press Releases

Telit News Center: Recent Press Releases

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 · Telit Receives Deutsche Telekom 5G Certifiion With more than thirty modules certified, customers have an extensive portfolio ranging from low [.] Read More. Telit FN980 Certified for Use on TMobile's 5G Network. July 13, 2021 Telit FN980 Certified for Use on TMobile's 5G Network Businesses and original equipment manufacturers (OEMs) are now able to leverage [.] Read More. .

Press Releases | GW Pharmaceuticals

Press Releases | GW Pharmaceuticals

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 · – If approved by the European Commission (EC), the label for EPIDYOLEX® will expand to include a third indiion in Europe – LONDON, Feb. 26, 2021 (GLOBE NEWSWIRE) GW Pharmaceuticals plc (Nasdaq: GWPH) ("GW", "the Company" or "the Group"), a world leader in discovering, developing and

Merging businesses in the EU

Merging businesses in the EU

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 · Your company purchases one or more other companies that are loed in another EU Member State (merger by acquisition) ... If the management of any of the merging companies receives feedback (in good time) from the employees, it will be included in the report. Independent expert report. This report (if required) is prepared for the owners of the companies involved. The report must be .

4 Stocks to Hold onto as the Mother Nature Wreaks Havoc ...

4 Stocks to Hold onto as the Mother Nature Wreaks Havoc ...

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 · With the acquisition of Edmunds under its belt, the company solidified its position in the used auto ecosystem. It aims to achieve 33 billion in revenues and sell two million units, annually ...

Home | The Pharma Data

Home | The Pharma Data

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 · Home | The Pharma Data. Takeda to Manufacture and Provide 150 Million Doses of Novavax'... Read More. Bayer's Eliapixant significantly decreased cough frequency in Phase IIb trial... Read More. Takeda Provides Update on Phase 3 PANTHER (Pevonedistat3001) Trial. Read More. AbbVie named to PEOPLE's "Companies that Care" list for third...

BREAKING: Buhari receives NDDC forensic audit report

BREAKING: Buhari receives NDDC forensic audit report

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 · Read Also: Forensic audit: contractors complete 76 NDDC projects In his remarks shortly before handing over the report, Akpabio, disclosed that the forensic audit covered a total of 13,777 ...

Amoy Diagnostics

Amoy Diagnostics

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Amoy Diagnostics Co., Ltd. (AmoyDx) is an RD based diagnostic company, focusing on molecular diagnostics for oncology precision medicine. With completely independent intellectual property rights of ADxARMS®, SuperARMS®, ddCapture® and HANDLE® technologies, AmoyDx has a marketleading portfolio of molecular diagnostic assays.

Frequently Asked Questions on Patents and Exclusivity | FDA

Frequently Asked Questions on Patents and Exclusivity | FDA

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 · An amendment to the description of approved method(s) of use claimed by the patent will be considered timely if it is submitted within 30 days of: (1) patent issuance, (2) approval of a ...

Investor News

Investor News

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 · Bayer strengthens drug discovery platform through acquisition of Vividion Therapeutics . READ MORE . August 03, 2021 . Not intended for and UK Media . Bayer's investigational P2X3 antagonist meets primary efficacy endpoint and shows favorable safety and tolerability profile . READ MORE . July 29, 2021 . Bayer Provides Update on Path to Closure of Roundup™ Litigation . READ .

Microsoft + Bethesda Deal Approved by EU USA Regulatory ...

Microsoft + Bethesda Deal Approved by EU USA Regulatory ...

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 · Microsoft's bid to acquire Bethesda in a billion deal has seemingly been approved by the regulatory agencies in both EU and USA.

Quidel Receives CE Mark for Savanna® Multiplex Molecular ...

Quidel Receives CE Mark for Savanna® Multiplex Molecular ...

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 · Quidel Receives CE Mark for Savanna® Multiplex Molecular Analyzer and Respiratory Viral Panel New Savanna® platform can analyze up to 12 pathogens, plus controls, from a single sample

Advicenne Receives MHRA Approval to Market Sibnayal™

Advicenne Receives MHRA Approval to Market Sibnayal™

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 · Advicenne Receives MHRA Approval to Market Sibnayal™ (ADV7103) in the UK for the Treatment of dRTA. Paris, France, 2 nd July 2021 – 7 am CEST – Advicenne (Euronext: ADVIC), a .

DBSE receives approval for exams, certifiion ...

DBSE receives approval for exams, certifiion ...

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 · DBSE receives approval for exams, certifiion equivalence with recognised boards: Sisodia PTI | Aug 13, 2021, 21:02 IST Deputy chief minister Manish Sisodia.

AstraZeneca receives EC approval for 39bn Alexion acquisition

AstraZeneca receives EC approval for 39bn Alexion acquisition

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 · AstraZeneca receives EC approval for 39bn Alexion acquisition. 06 Jul 2021 (Last Updated July 6th, 2021 12:22) In the US, Japan and multiple other countries, AstraZeneca already received competition clearances for the acquisition. ...

WuXi Receives Manufacturing Approval for German Drug ...

WuXi Receives Manufacturing Approval for German Drug ...

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 · WuXi Receives Manufacturing Approval for German Drug Product Facility. German health authorities issued WuXi Biologics a License of Manufacturing Permit for .

Compliance Checklist: Joint Commission's Imaging Standards

Compliance Checklist: Joint Commission's Imaging Standards

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EP 16 (Applies only to MRI) Access to the MRI area is restricted.* all staff and patients are screened prior to entering the MRI area.* there are controls in place to prevent unauthorized access to the MRI area* warning signage is posted at the entrance to the MRI scanner* signage is posted indiing that the magnet is always on (as applicable)* EP 4 (Applies to CT ...

Press Release Overview |

Press Release Overview |

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 · Boehringer Ingelheim receives approval for Aservo® EquiHaler®, industry first equine asthma therapy 09. Jan 2020 01:00 pm: Boehringer Ingelheim Partners with Enleofen to Develop FirstinClass AntiIL11 Therapies for a Range of Fibrotic Diseases 03. Jan 2020 09:00 am: Introducing DiaTEC, a new purifiion technology for Ingelvac CircoFLEX®

CS533E CP533E

CS533E CP533E

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® 3054C Turbocharged ... The 3054C engine meets EU directive 97/68/EC Stage II emission requirements. Dual Pump Propel System High tractive effort and gradeability for outstanding productivity in tough appliions. Dual propel pumps. Dual propel pumps provide separate, balanced hydraulic flow to the rear wheel axle and the drum drive motors. Provides superior gradeability on steep slopes ...

 | Global Loions | Offices Facilities

| Global Loions | Offices Facilities

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's global reach and presence is unmatched in the industry. Headquartered in Deerfield, Illinois,, we serve customers around the globe. Our manufacturing, marketing, logistics, services, research and development (RD) and related facilities, along with our dealer loions, total more than 500 loions worldwide.

Development Approval Process | Drugs | FDA

Development Approval Process | Drugs | FDA

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Get to know FDA's drug development and approval process ensuring that drugs work and that the benefits outweigh their known risks.