Welcome to ALP Pharm

Email: lisa@alliancepharm.com , gary@alppharm.com.cn

ALP Pharm Beijing Co., Ltd. was found in Sep.2006, began to manufacture some APIs in the partners facilities since 2007.

Some of our APIs have been approved by EU regulatory countries, US FDA, Health Canada, TGA, New Zealand, Isreal, Mena,Latam region, Chile, Colombia, Mexico, Brazil, Singapore etc.

ALP Pharm‘s rapid business growth has been based on the knowledge and integrity of its core management team, technical and regulatory executives from China, the U.S., and EU countries.

Our professional regulatory compliance expert have more than 10 years cGMP experience, all have much experience during many times US FDA inspection and EU inspection. They are now working hand in hand to ensure that all documentation meets the necessary requirements of authorities and customers in North America and Europe.

For many APIs, ALP Pharm Beijing Co Ltd is the DMF holder and controls all the key points on manufacturing and quality control which helps much to the ANDA holder or MA holders in all regulated markets.

ALP Pharm Beijing Co Ltd did great sales for the whole regulatory markets from 2006 to now.
ALP Pharm Beijing Co Ltd did great cGMP compliance work for API contract manufacturers, all pass FDA inspection and /or EU authority inspections successfully.

ALP PHARMACEUTICAL INC is founded in USA in Sep.2022.
ALP PHARMACEUTICAL INC Business Operations: cGMP Regulatory Affairs communication with US FDA.