Fast won the AS9100D quality management system certification

On August 27, 2018, the awarding ceremony of the Fast AS9100D aerospace quality management system certification ceremony was held in Xi'an High-tech Factory. Zheng Bin, manager of the North Zone of Bureau Veritas, issued a certificate for Fast. Yan Jianbo, party secretary and chairman of the group company, attended and spoke.

Certificate presentation ceremony site Certificate presentation ceremony site

As a leader in the automotive transmission system, Fastter has obtained the AS9100D certification “passport”, which will better promote the high-quality development of the company.

Group photo after the certificate issuance ceremony Group photo after the certificate issuance ceremony

In the new era, new environment and new requirements, Chairman Yan Jianbo emphasized that the integration of the integration will make up for the shortcomings, and the flexible use of the functions will be carried out to comprehensively improve the quality management level and enhance the core competitiveness of the enterprise.

AS9100D is an aerospace standard developed on the basis of ISO9001 quality system requirements. This standard is intended to establish a unified quality management system requirements for the aerospace industry.

Reading volume: Source: Fast Author: Zebian

Apixaban API And Intermediates

Apixaban is a novel oral factor Xa inhibitor jointly developed by Bristol-Myers Squibb and Pfizer under the trade name Aldol, which is a novel oral anticoagulant. Apixaban prevents thrombin production and thrombosis by inhibiting an important clotting factor, Xa. On April 26, 2007, Bristol-Myers Squibb and Pfizer announced a collaboration to develop apaxaban, a new oral anticoagulant owned by BRIstol-Myers Squibb, as an upgraded alternative to warfarin. Under the agreement, Pfizer will make an upfront payment of $250 million to Bristol-Myers Squibb for 60 percent of the total development cost of apisaban, effective January 1, 2007, and Bristol-Myers Squibb will pay the remaining 40 percent, resulting in co-development and marketing rights for the drug. In May 2011, Apixaban was approved for the prevention of venous thrombosis in adults undergoing elective hip or knee replacement surgery in 27 European Union countries, Iceland and Norway. On 20 November 2012, the European Commission approved aldol (apisaban) for the prevention of stroke and systemic circulation embolism in adult patients with NVAF who have one or more risk factors for wind Chemicalbook. Subsequently, FDA of Canada, Japan and the United States approved Aldol? Apixaban is indicated for the prevention of stroke and systemic circulation embolism in adult patients with nonvalvular atrial fibrillation (NVAF) with one or more risk factors. On April 12, 2013, ELIQUIS (apisaban), a new Anticoagulant Drug jointly developed by Bristol-Myers Squibb and Pfizer, was officially launched in China. Aldol is a novel oral factor Xa inhibitor for the prevention of venous thromboembolism (VTE) in adult patients undergoing elective hip or knee replacement. Its marketing provides a safe and effective new alternative for clinical anticoagulation after orthopedic surgery, and brings good news to patients undergoing elective hip/knee replacement in China. Clinical studies have demonstrated that two oral doses of enoxaparin per day are better than one subcutaneous injection of enoxaparin 40mg per day. Apixaban 2.5mg is more effective in preventing venous thromboembolic events after hip or knee replacement surgery without increasing the risk of bleeding.


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