GMP Production Facility

CGMP Production Facility

We are operating in a brand new facility, which allows HNSP to be one of the leading companies into the CGMP manufacture of bioactive peptides.
Our modern facility offers 5,700 square meters (613,542+ square feet) of production area and laboratories, for the CGMP manufacture of Sterile API Peptides, including lyophilization and packaging under sterile conditions. Six facilities have passed the CFDA CGMP audit (including two Peptide API facilities and four Lyophilized Injection facilties); Non-sterile API manufacturing facility received US FDA approval in 2013; Italian authority AIFA will inspect Thymalfasin API and FD in Jan/Feb 2016; US FDA may inspect Bivalirudin API and FD in 2016. Also, HNSP’s new production line for Cartridge formulations is ready for production. 
友情链接:幸运农场  北京赛车pk拾网站  澳彩网彩票  创元彩票  幸运农场官网  幸运农场  新世佳彩票  

免责声明: 本站资料及图片来源互联网文章,本网不承担任何由内容信息所引起的争议和法律责任。所有作品版权归原创作者所有,与本站立场无关,如用户分享不慎侵犯了您的权益,请联系我们告知,我们将做删除处理!