Stericon is an ISO 9001 company certified by Det Norske Veritas, Norway . Our range of solutions have also received the CE certification which certifies that the solutions are manufactured under strict GMP conditions and guarantees our customers total quality. We are committed to provide quality products as per customer and market requirements on time every time thereby ensuring customer satisfaction. |
We follow strict and mature processes to ensure that quality is maintained at the highest levels. A separate quality control department continuously monitors the quality of raw material , packing material, in process and finished products . It is well equipped for conducting chemical &z microbiological tests and also pyrogen and sterility tests. Strict quality control processes have been established, which include sampling and analysis, shelf life studies and internal GMP audits.
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The manufacturing process occurs under stringent quality controlled conditions. Stericon is equipped with state-of-the-art equipment covering every step of the process, from manufacturing through washing, sterilization, filling and packing.
All raw and packing material is carefully selected from reputed vendors and only the most stable ingredients are used. A master formula is available for all products and a batch manufacturing record (BMR) is generated for every batch, which ensures traceability of all material. Standard operating procedures for all activities and equipment are available which are periodically reviewed and updated.
All incoming materials are sampled and analyzed as per pharmacopoeial and in house standards. In process quality control checks are done and finished goods are released only after analysis and approval. Stability studies are carried out periodically to establish the rationale of the product.
