Our chemicals are processed using the best available raw materials and modern production techniques under the strict guidance of our skilled team of professionals. We follow a strict and detailed Standard Operating Procedure (SOP) in all our manufacturing, Quality Control (QC) and Quality Assurance (QA) activities. As a Drug Licensee holder DL 25/20/95, the procured material is also stringently tested on several quality parameters to avoid any kind of discrepancy in the offered range.
Our entire process is divided into 3 major verticals namely – Production, QA & QC and Packaging. We have modern machinery and state-of the art infrastructure to assist our professional team in meeting our goals in designated time frame. Our professionals are hard-working with high expertise and knowledge. They channelize all their skills and energy towards making the company more popular in the market. Regular seminars and training sessions organized by us help in keeping them well-versed with the prevailing and changing industrial trends.
Each and every stage is closely monitored by them to ensure flawlessness. Being a market leader is not an easy task but our customer-first approach has helped us to achieve that dream. Our ultimate aim is to produce zero defect product and all our systems should act as filters at all levels to ensure that our products are of good quality and fulfill the individual requirements of our customers. We follow Ethical Business practices, on-time delivery and Client-first approach to maintain relations with all our business partners.
Manufacturing Operations
Our state-of-the-art fully automatic and continuous manufacturing facility is well equipped to meet the growing needs of our clients. The facility is spread over 80,000 sq feet area and the plant is designed as per cGMP norms with sufficient space for dedicated operations.
All the equipments are of SS316 with up to 50 feet Packed Distillation column height. Our Finished products are packed in Clean room environment with 0.3 Micron Hepa filters and bear a Class ‘D’ Classification. Our Dedicated Raw Material and Finished Product Store ensure there is no chances of Cross Contamination.
Quality Control & Quality Assurance
We understand that manufacturing of high purity products require High end Analysis Devices. Our customers are assured of receiving zero fault goods, every stage of production from vendor approval of raw materials to production , analysis and packaging is closely monitored as per specifications. All the processes are well documented as per SOPs. These filled documents are regularly checked by QA department to ensure Zero Default Product. In case any discrepancy is observed Training is imparted to the concerned department so that it is not repeated again.
We understand that manufacturing of high purity products require High end Analysis Devices. Our customers are assured of receiving zero fault goods, every stage of production from vendor approval of raw materials to production , analysis and packaging is closely monitored as per specifications. All the processes are well documented as per SOPs. These filled documents are regularly checked by QA department to ensure Zero Default Product. In case any discrepancy is observed Training is imparted to the concerned department so that it is not repeated again.
The role of Quality Assurance is to coordinate the development and maintenance of the Company’s quality procedures and systems. This is achieved by a combination of systematic sampling, testing, validating, monitoring and auditing of materials, facilities, systems and procedures which can influence the quality of the Company’s products throughout their shelf life.
Good Documentation Practices (GDP)
There are Standard Operating Procedures duly documented and authorized, for all operations including production, Quality Control, Materials Management warehouses and distribution, safety, environmental controls, housekeeping, sanitation and engineering. The role of quality assurance is to ensure that these procedures are adhered to and records are maintained. Any deviation or discrepancy is investigated and documented. Corrective action is taken wherever necessary.The four levels of documentation are represented in the pyramid below.
The Quality Head reviews and approves all requests for amendments to existing documents and the development of new procedures, processes, and policies, which is addressed through change control procedures.
Staff is not permitted to make any amendments to documentation without the prior consent of the Quality Head and if each change is routed through change control
When new or modified policies, processes and procedures are instituted, staff requires retraining.
All procedures are reviewed once in 3 years. The responsibility for review lies with the quality head and concerned departments. The quality head is responsible for the distribution of new documents, retrieval of old documents and maintenance of records of amendments.