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Medicine Film Drug Machinery
Infusion Medicine Machinery（中文站有输液剂机械的三级分类）
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Fan
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Gasket
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Safety Cabinet
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Insulin Pens / Blood Glucose Management Devices
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Animal Experiment Instrument
Injection & blow molding machines
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Incubator Equipment
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Palletizing equipment
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Topical / Gynecological / Intimate Drug Delivery Devices
Desiccants
Other Life Science Instrument
Bottle Filling Line
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Lifting Charging Machine
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Inhalant Packaging
BFS Bottlepack Machine
Weighting Equipment
Blister Packaging Machine
Pharmaceutical Paper
Other Pharmaceutical Outer Packaging Equipment
Packaging bag valve
Container Sealing Machine
Glass Tube
Multi-functional Bottle Packaging Machine
Medical Aesthetic Freeze-Dried Powder Vials
Sachets Cartoner Packing line
Primary Packaging
Other Pharmaceutical Inner Packaging Equipment
Aluminum Caps & Aluminum-Plastic Combination Caps
Sterile Bags / Breathing Bags / Sterilization Bags
Medical Device Packaging / Bioconsumables Packaging
Dispensing Bottles
Blister Packaging
Pharmaceutical Plastic Films / Composite Film Bags
Accessories
Ampuls
Other Packaging Materials
Jilin Beisha Pharmaceutical Co., Ltd.
15
Years
Shop
- Shop
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Company Profile of Jilin Beisha Pharmaceutical Co., Ltd.
Basic Information
Company Name
Jilin Beisha Pharmaceutical Co., Ltd.
Year of Establishment
1993
Enterprise Size
100-500
Company Introduction
Jilin Beisha Pharmaceutical Co., Ltd. produces Vitamin E, 50% Vitamin E powder and Taurine. It is certified of ISO 9001, ISO 22000 and EU FAMI-QS.
Nanhai Beisha Pharmaceutical Co., Ltd. produces various Sulfonamide APIs, intermediates of 7-AVCA and LK-Penicillin Sulfoxide since 1993. It is certified by SFDA, ministry of agriculture, US FDA and CEP.
Main Competitive Advantages
N;
Postal Code
132101
Website
www.beisha.com
Milestone
In 1992：Nanhai Beisha Medical Material Factory was established.
In 2003：The company name was renewed to be Nanhai Beisha Pharmaceutical Co., Ltd.
In 2004：The GMP certificate for human use issued by CFDA was obtained.
In 2006：The GMP certificate for veterinary use issued by MOA was obtained.
In 2008：The CEP certificate for Sulfadimidine issued by EDQM was obtained.
In 2010：Nanhai Beisha was inspected and accepted by US FDA. Jilin Beisha Pharmaceutical Co., Ltd. was established.
In 2011：Nanhai Beisha was approved by the Indian DCGI.
In 2013：Nanhai Beisha was re-inspected and accepted by US FDA again.
In 2014：Jilin Beisha was approved for the FAMI-QS and Indian authentication.
In 2017：Nanhai Beisha was re-inspected and accepted by US FDA again.
In 2018, DMF was assessed and approved by many of the European authorities. Jilin Beisha was inspected and accepted by US FDA.
In 2019：Nanhai Beisha was inspected and accepted by Japanese PMDA.
In 2020： Nanhai Beisha resumed the manufacturing of Chloroquine phosphate for fighting against COVID-19.
Trading Ability
Business type
Manufacturer
Main Sales Market
North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa,
R&D Capacity
Own Brand,
Contract Customization
Other,
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