Dr Vishys SIA
Supplying a comprehensive range of Medical and Pharmaceutical Products.
Regulatory
Dr Vishys has tied up with dedicated regulatory affairs department at a research facility in India responsible for the registration of products in various countries. The team of regulatory affairs experts plays a pivotal role from initiation to completion of the project ensuring compliance with applicable laws and regulatory throughout the process. We have successfully submitted numerous dossiers for regulatory and semi regulated markets.
At Dr Vishys we believe in “Excellence through Quality” . Dr Vishys maintains strict quality parameters for the manufacturing and distribution of products.
Dr Vishys Sia has exclusive tie up with a Research Company having independent Corporate Quality Assurance Department responsible for quality affairs.
Achieved head of state position through our supreme levels of quality. Dr Vishys strives to deliver highest level of quality and customer satisfaction. ISO 9001:2008 Certification and ISO / IEC 17025:2005 Accreditation explain the efforts to achieve maximum quality level. Quality Assurance is a measure of the degree of sophistication of managerial, scientific and technical tools used in the plan and execution of product process of any industry. In the pharmaceutical industry QUALITY is the most fundamental task of Total Quality Management.
We at Dr Vishys SIA are committed to ensure that every product we manufacture and distribute meets with and conform over its shelf life to internationally accepted standards of quality, purity, efficacy and safety. Dr Vishys quality focus encompasses all areas of operation – from procurement of the best raw materials, to optimum manufacturing technology, to precise delivery of the customer’s requirements – thus ensuring a rapid access of both domestic and global markets. All the systems are well documented and are implemented by an expert trained staff with a line of reporting that is independent of manufacturing.
Dr Vishys have exclusive relationship with facility having state of the art laboratory with the advanced infrastructure and procedures to support a stringent quality policy. At the manufacturing site, the latest analytical instruments and firmly monitored quality assurance and quality control systems ensures consistent quality of the products. There are regular validations of processes, test methods, water and environment, as well as periodic calibration of all instruments, to guarantee product output of consistent top quality. Vendor evaluation and selection is carried out as per stringent quality, product, manufacturing, service and delivery parameters to ensure the highest quality raw materials.
The Quality Assurance Department has accomplished and qualified personnel, who constantly monitor quality parameters and performing systematic sampling and testing at every stage from raw materials, through each process of intermediate and finished products.
A full-fledged Quality Control Laboratory which follows Good Laboratory Practices and incorporates the most modern testing equipment, in order to perform the stringent quality analytical tests prescribed by different national and International Pharmacopoeia is available at the facility