Welcome to Arion healthcare.

Developmental Quality Assurance

At Arion Group quality is the way of life. It is not just about SOPs and the hardware. It is an encompassing culture that is the foundation of all business decisions.

Shape
Thumb Thumb

We believe that the key to strengthening the foundation of a responsible brand lies in consistently achieving high standards of quality in everything we do. Quality is embedded at every stage of our operations, including procurement, manufacturing, delivery and safe product disposal. Our focus over the past few years has been to enhance our Quality Management Systems to meet and exceed the current expectations of regulatory authorities. (Such as WHO, Asian and African countries , CIS, LATAM etc.)

We’re committed to achieving zero-defect and implement strict quality controls to ensure that every product released from its manufacturing facility adheres to all applicable quality and regulatory standards. This reputation of delivering consistently high-quality products has helped us to be considered as one of the key partners of choice for multinational Government and Non-Government institutions globally. We conduct regular vendor audits to ensure adherence to relevant quality standards across its value chain. The Quality by Design (QbD) team and Development Quality Assurance (DQA) team work closely with the R&D function to monitor quality during clinical trials, tech transfer and developing molecules.




QUALITY

QUALITY AT ARION GROUP IS PATIENT CENTRIC AND INFINITE. Quality and Arion Group are synonymous.

Quality par excellence is our defining attribute at every location and our every operation.

Our Quality Management Team is an overseer, which ensures that each of our products stand true to the global standards of quality, purity, efficacy and safety. The quality unit at our sites are guided by a Corporate Quality Assurance (CQA).

CQA ensures that the latest updates in Good Manufacturing Practices (GMP) are being translated into our policies, guidelines and Standard Operating Procedures (SOPs).
Quality unit at respective sites further ensures that these guidelines are implemented to consistently deliver top-notch products across all territories.


Thumb Thumb

In addition to this, the manufacturing sites are regularly audited by CQA to ensure 24x7 compliance and conformance. In addition, our quality management team is also involved in overseeing compliance with respect to Good Clinical Practices (GCP) and Good Laboratory Practices (GLP).

To maintain quality standards, we have placed compliant procedures and system at each of our manufacturing facilities. These procedures and systems are in compliance with the requirements of the Current Good Manufacturing Practices (cGMP) and our systems meet the global standards of regulators.

Our well-trained and competent colleagues ensure strict adherence to systems and procedures.

Our persistent commitment to quality also gets extended to our business partners and service providers. We insist that they comply with global quality standards which are aligned with our own. Our benchmark of quality is inspired from the best of global practices. We continuously evolve and upgrade our quality systems to match with the evolving dynamics of the global environment.

We are committed to deliver the highest level of quality and our facility and legal entities is steadfast to meet the impeccable standards that are expected from a global pharmaceutical company.