Formulation Research & Development
With the similar facility having miniature machines ensuring replication of the process, all the dosage forms are developed in FR & D with materials, process and control, specifications and their stability study with focus on creating value through innovation, by formulating and developing novel products.
Accord believes that quality is achieved through continuous individual & collective team effort of all the personnel, suppliers and contractors working for the company.
Production
The production department is well equipped with machines and equipment of latest technology. The tablet compression machine, capsule filling machine, tube filling machine and liquid filling machine are fully automatic to ensure the precision. The packaging unit is automatic too. All manufacturing processes are clearly defined, systematically reviewed and are shown to be capable of manufacturing medicinal products of the required quality consistently as per recommended specifications.
Quality Control
A separate Quality Control Department is working with chemical, instrumentation and microbiological section for analysis of all input raw materials, packing materials, intermediate and finished products with sophisticated instruments like High performance liquid chromatography (HPLC), Fourier Transform infrared spectrophotometer (FTIR), Auto sampler dissolution machine, Karlfisher titrator and many more. The department operates under Pharmacist, Chemist, and Microbiologist.
Quality Assurance
The quality assurance department is constantly working to ensure the quality products. They are basically involved in technology transfer, calibration and validation, Documentation, Quality improvement plans, assuring quality of the products.
Stores
All the specified raw materials and packing materials are procured from approved vendors only. Accord has systematic storage and area for storage of raw, packing and finished goods with 10500 sq. ft area. Here is provision of separate sampling booth for Active Pharmaceutical Ingredients & excipients with separate dispensing booth for tablet/capsules & Liquid/semi solid dosage forms.
AHU/RO/ETP
Accord has proper implementation of Building Management System (BMS) for Tablet and Capsule section and Environmental monitoring System (EMS) for Liquid and Semi solid for controlling and monitoring of Temperature, Humidity and pressure difference in production during dispensing, manufacturing and packing of the products. The Reverse Osmosis-Electro Deionization (RO-EDI) water purification system and Effluent Treatment Plant (ETP) confirms the commitment towards quality and environment.
