 Drug Regulatory Department
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| The company posses Capability for preparing technical Dossiers as required by Individual countries and DMR Our facilities are constantly upgraded to comply with European Inspection making us strategically poised to enter regulated markets adopting hi-tech facility. |
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Dedicated R&D Team |
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The company firmly believes that a strong R&D focus will provide the right edge and sustained future growth. The R &D team comprising of competent personnel is equipped to undertake basic and applied research in the field of pharmacology, toxicology, fermentation, Development of Dosage forms, Normal Drug Discovery, Biotechnology . The stress is on creating new molecules.
Continuous in-house research is conducted to improve product properties and process parameters with a quest to provide defect free products. The R&D Department is manned by more than 20 highly experienced R&D personnel. The dedicated R&D team is well supported by latest equipment and facilities required for high research and scale-up work |
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Technology |
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| The company keeps itself abreast with technological development to ensure required purity in all sequences of products. |
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International Compliance |
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Hi-tech production facility:- The company has sophisticated modern manufacturing Plants adopting hi-tech facility. Acquisitions, transfer of technology, introduction of New Products is an ongoing process at SWISS. |
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Both its products and process are reviewed periodically and upgraded for compliance of Quality, Cost and Safety - All from customer's point of view and inline with Business Ethics to health care industries. |
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Absolute Commitment to Quality: - Quality has been one of our activities to ensure products meet with International Standards. Quality assessment of Raw material and Finished product is an indispensable part of Production Process of Marketable Products. To ensure Total Quality Management, our Quality Assurance Department is an Autonomous Unit. Procedures that support a stringent quality policy are in place. Well Documented systems are vigorously implemented and maintained and monitored by trained staff. |
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Regulatory Compliance |
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| Quality adherance at every step in manufacturing |
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Complete compliance to cGMP procedure and record maintenance as per ICH guidelines. |
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Committed Formulation Development Department. |
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Well equipped Quality Assurance Department ensures stringent maintenance of quality standards. |
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Regulatory Department capable of handling common technical documents and dossiers for any country. |
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