Abhilasha Pharma Pvt. Ltd. is a pharmaceutical company that produces a wide variety of Acitve pharma ingrediants(bulk drug) Some of the API’s that are manufactured by Abhilashapharma.
Abhilasha Pharma got the Manufacturing license in 2007 and number is G/25/1788. The manufacturing license is renewed in 2012.
Abhilasha Pharma having the WHO cGMP certificate from 2010 and Re-audit the facility in 2015.
Korean Drugs and Food Administration (KFDA) Audited the facility on March-2013 and Approved the facility.
ISO (TUV) certificates initially got in 2008 and Re-audited the facility by ISO (TUV) agency in 2014.
Facility has been granted "Written confirmation" certificate for export of API to European union.
The certification Number of EU-GMP (Written confirmation) is WC-0325 and certificate valid up to DECEMBER 2017.
Its large product line serves as Anti-septic, Anti-inflammatory, Anti-fungal, Anti-diabetics, Antihistamine, and Cardiovascular remedies.
Abhilasha Pharma has its state-of-art CGMP WHO approved manufacturing unit are located in Ankleshwar Gujarat, India where manufacture of Active Pharmaceuticals ingredients and Intermediates outfitted with. With the use of innovative technology and advanced Drug manufacturing unit, it produces Active Pharma ingredients that meet Pharmacopoeial standards. Today, Abhilasha Pharma is leading drug manufacturer unit in India.