OUR VISION
Our vision is to build OCTANCE HEALTHCARE into a leading specialty pharmaceutical company with a global presence. Through organic growth and strategic acquisitions, we will continue to develop the business and maintain the high standards of ethics and responsibility that are central to the way we operate.
The OCTANCE GROUP is implementing integrated strategies and plans to achieve its goal of becoming a “TOP PHARMACEUTICAL COMPANY” by the late 2025 as our vision is to become an admirable HEALTHCARE company to ensure health for everyone, everywhere. We are committed to improving people’s lives through our existing products and our extensive and differentiated pipeline. Our aim is to provide patients with better access to high-quality, affordable medicines in key therapeutic areas. Provide quality healthcare products and services for the benefit of humanity in the best possible way through innovation and diversification.
QUALITY MANAGAMENT SYSTEM
The QMS of OCTANCE HEALTHCARE PRIVATE LIMITED is established in a frame to describe its operations in different documents and practices which is based on the principles of PICS and WHO guidelines. The Quality Manual describes the Quality Policy of OCTANCE HEALTHCARE PRIVATE LIMITED.
The responsibilities for the technical aspects of Quality Assurance are defined in Quality Manual. It encompasses all activities necessary to generate, maintain and verify the quality of drugs.
The Quality Assurance of Every manufacturing plant consists of Quality Control, Quality Compliance and Quality Surveillance. The main tasks and duties of Quality Control have been
Described in the Quality Manual and relevant SOPS’s. The Head of Quality Assurance or his delegates are responsible for releasing drug substances, Excepients, dosage forms and packaging materials.
Quality Compliance is responsible for IPC, GMP co-ordination and training. Performances of routine GMP checks are done as per need. Monitors to respect GMP regulation in the manufacturing by instant checks of Batch Record completion visual checks of cleaning and working place, line clearance, performance checks of balance and other equipment.
Quality Surveillance is responsible for the implementation of the Quality Management System in different areas in collaboration with different departments. Quality Surveillance play active role in conducting external and internal audits with their follow- ups.
The Quality Manual describes how testing instructions are established and used. The testing instructions include the specifications and testing methods. The testing instructions are binding for release testing and for follow-up stability testing. A routine inspection is being done in the name of “Self Inspection” mainly concerned with safety, sanitation and infrastructural facilities leading to GMP including documentation.
Supplies of raw materials are mainly obtained from approved suppliers. We select and evaluate the supplier as per procedures. This procedure is also applicable in case of supply of Primary and Secondary Packaging Materials.