At Arion Group quality is the way of life. It is not just about SOPs and hardware — it is an encompassing culture that forms the foundation of every business decision.
Quality begins right from the initial stages in the form of Developmental Quality Assurance (DQA) when R&D starts developing a new product.
Arion Group Quality Control as a centre of excellence assures a culture of compliance and follows systematic interventions to consistently meet or exceed quality standards.
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 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.
Maintaining Global Manufacturing Standards
In addition to this, the manufacturing sites are regularly audited by CQA to ensure 24×7 compliance and conformance. Our quality management team is actively involved in overseeing compliance with Good Clinical Practices (GCP) and Good Laboratory Practices (GLP).
To maintain quality standards, we have implemented compliant procedures and systems at each of our manufacturing facilities. These procedures and systems are fully aligned with Current Good Manufacturing Practices (cGMP) and global regulatory requirements.
Our well-trained and competent professionals ensure strict adherence to systems, operational protocols, and compliance-driven procedures across all manufacturing processes.
Our commitment to quality extends to our business partners and service providers. We continuously evolve and upgrade our quality systems to align with global best practices and the changing dynamics of the pharmaceutical industry.