At Clixson Bio Pharma, the Quality Assurance and control is a stringent procedure intended to determine that the manufactured products should strictly adhere to a defined set of quality criteria or meet the requirements of the client or customer, as per the International Quality Control Standards.

In order to implement an effective Quality Control program, we have predefined specific Quality standards that our products and services deliver. These procedures are clearly mentioned in our SOP. We Collect real-world data.

Clixson Bio Pharma is an exporter of ethical and generic medicines worldwide. Our products are manufactured in WHO, GMP, GLP Compliance and ISO certified.

Our Products (Branded and Generics Formulation) exports to many countries Globally, Which includes , African & South –East Asian Countries.

Currently we are exporting different products to African & South –East Asian Countries.

We produce various dosage forms encompassing a vast range of therapeutic categories. Our formulation development team and regulatory department are focused on Latest molecules & Product Formulation.

We are the exporters of Pharmaceutical Products like Tablets, Capsule, Sachets, Syrups, Nutritional Supplements (Dietary Products),Herbal Supplements, and Cosmetic Product etc.

Clixson Bio Pharma comprises of a hitech and huge capacity of manufacturing unit based in INDIA. With advanced infrastructure facilities including Transformer-power-station, water storage and treatment facility with total close loop system, requisite constructed plant and machineries, air-handling-units, effluent treatment plant, etc. The unit has qualified, competent, experienced and trained personnel to handle the production of antibiotic dosage in India.

We manufacture using properly designed, installed, validated and maintained equipments under supervision of qualified personnel. These are operated and cleaned as per SOPs. All units installed for manufacturing are as per Good Manufacturing Practice and revised schedule-M. Sufficient space as per cGMP has been provided for the storage of raw materials and packing materials, manufacturing, testing, in process controls, etc.

Adequate measures have been taken to ensure the quality of the products such as process and utility validations, proper sanitation, proper maintenance of equipments. All activities are performed by trained and skilled personnel under supervision of competent personnel and necessary records are maintained. Stability studies are carried out as per WHO guidelines. In the plant, cGMP norms are followed. Measures are taken to prevent cross contamination.