◆In Oct 2012, The U.S. branch open business formally
◆In Nov 2011, The U.S. branch is registered and established.Named as Lu'an Pharmaceutical (USA) LLC.
◆In May 2003, Paracetamol lines passed Chinese GMP Certification.
◆In Sep 2003, newly upgraded P-Aminophenol line was put in operation.
◆In Mar 2004, Paracetamol Fluid Bed Granulation Workshop housing Unique Glatt Granulator in China was put into operation.
◆In Apr 2004, Production Capacity for Paracetamol increased to 24000 tons a year by new Paracetamol workshop put into orperation.
◆In May 2004, Paracetamol line passed EDQM Site Inspection.
◆In Dec 2005, Paracetamol granulation facility passed GMP Site GMP Certification made by Germany Bavarian Government.
◆In Jan 2006, DMF for Paracetamol for Rx and Paracetamol DC Rx was filed in US FDA.
◆In Nov 2006, Registration Certificate for Paracetamol was issued by Russia Authority.
◆ In Dec 2006, Soft gel production line was put into operation with annual capacity of 500 million soft gels.
◆In Feb 2007, GMP for Health Product was granted.
◆In Feb 2007, COS was renewed succesfully.
◆In Feb 2007, India DCGI renewed Registration Certificate.
◆In Jun 2007,ISO14001 ISO9001 OHSAS18001 was approved.
◆In Feb 2008,Chinese GMP for Paracetamol was renewed by site GMP inspection.
◆In May 2008,Weifang Lu'an Import & Export Co., Ltd. set up as subsidiary of Anqiu Lu'an Pharmaceutical Co., Ltd. and fully responsible for export Paracetamol products made by Anqiu Lu'an Pharmaceutical Co., Ltd.
◆In Jun 2008, Paracetamol Dosage Form workshop passed Canadian MOH CGMP Inspection.
◆In Aug 2008, Passed EHS Audit conducted by several multinational pharmaceuticals worldwide.
◆In Oct 2008, Paracetamol DC workshop passed Re-inpsection made by Germany EU Inspection.
◆In Oct 2008,Paracetamol workshop passed Re-inspection made by EDQM.
◆In Feb 2009, DMF for Paracetamol for OTC was filed in USFDA.
◆In Feb 2009, Developed Fast Soluble Paracetamol Tablets.
◆In Mar 2009, Paracetamol Spray Dry Granulation Workshop was put into operation.
◆In Sep 2009, Paracetamol API Workshop and Paracetamol DC Workshop passed US FDA site GMP Inspection.
◆In Nov 2009, New Paracetamol API Workshop is started gound construction. It is designed in c GMP and annual capacity of 16000 tons, that allow total capacity of Paracetamol API increased from current 24000 tons to 40000 tons. It is expected to put into operation in 2010.
◆In Apr.2011,the workshop#5(Capacity 160000mt) put into use
◆ In Nov.2011,the facilities passed the re-inspection by US FDA
◆ In Feb.2012, the facilites passed the site GMP inspection by Korea FDA
◆ In Mar.2012,No.5 workshop passed the site GMP inspection by FDA of Chinese
◆ In Jan.2013,the workshops of NO.1,NO.2,NO.3 passed the site GMP inspection by FDA of Chinese Shandong Province