ISO Approved Pharmaceutical Quality System
|Our commitment to quality and regulatory affairs is in one of full compliance to International and National norms and regulations. Dedicated Quality Assurance Department and strict quality control procedures guarantee consistent quality of all processes and products. We continuously monitor our suppliers, raw materials, in process controls, intermediates, finished goods, packaging, labeling, shipment, delivery and adhere to ISO 9001:2000 and OHSAS 18001:2007 quality standards to ensure consistent levels of quality.
ISO 9001:20015 Quality Management Systems
ISO certifies Quality Management Systems and this is the core value of an ISO 9001:2008 certification. A pharmaceutical manufacturing company that has achieved an ISO 9001:2008 certification has achieved the highest-level Quality Management System Certification.
OHSAS 18001:2007: Occupational Health and Safety Management Systems
At a time when greed, materialism and apathy have overtaken the basic qualities of human life, Ganesh group plays a proactive role in preserving marvels of mother nature for future generations. To attain our objectives we have indigenously developed process and equipment that either reduce or completely eliminate pollution.
ISO 14001:2015 Environmental Management Systems
Our customers and Outsourcing Sponsors are the direct benefactors of our ISO certification by assuring, through independent auditors, we are compliant to a proven Quality Systems Model. The ability of a pharmaceutical manufacturer to consistently provide quality products and regulatory compliance is defined by their ability to manage themselves and their processes.
ISO certification assures our customers that in addition to meeting cGMP requirements for manufacturing, we will meet the their needs for product design, product development, production, installation and servicing.
Compliance to ISO standards is voluntary and most pharmaceutical manufacturing companies choose not to become certified because of the added level of Quality System oversight that FDA current good manufacturing practices (cGMP) do not require. There are different levels to the ISO 9000 certification. ISO 9001:2008 is considered by many to be the most difficult to certify against and our certification includes the all-important Product Design portion of the standard.
Environment protection is our core concern.
Click here for our Quality policy
Click here for our Environment policy