Welcome to KVS Technologies
KVS Technologies is a partnership company promoted and managed by Kalpesh R. Vaghela and Shankar P. Sapavadiya. both having work experience of about 25 years in India and Abroad. Since last 18 years main area of interest is with pharmaceutical industries. KVS Technologies is a team of dedicated, talented engineers whom you can trust for your regulatory requirement.
Dedicated Software Validation Service provider Company KVS technologies 10 year old. It has 20 years of experience (Parent company Infra Control Systems) and partner experience is of 30 years.
KVS Technologies Provides Quality Validation, Services to the Pharmaceutical, Biotechnology and Medical Device Industries. We have the team of talented and committed people to take care and provide excellent services for all type of regulatory requirements.
We offer a full list of services such as Software Validation of Computer System, HPLC –PLC , DCS-SCADA , SAP-ERP Software, BMS. Training and 21 CFR Part 11 Compliance Audit and much more. Quality Validation Work, complete responsibility from start to finish, personalized support and the success of your projects at best price are the foundation of our company.
Why Choose KVS Technologies
As KVS Technologies we work as Your Validation Partner, we work with commitments. Our rooted knowledge with the industries, stems from our continuous learning, a key to our market leadership.
BMS Validation System
BMS Validation System, Sauter, Honeywell, Siemens, Johnsons.
Clinical Research Software
– Clinical Trial application software, PE Access.
– SAS, WIN Non Lin, Application Software Validation.
Regulatory compliances Services
Contract Laboratory or commercial testing labs or third party testing labs are driven by their customer and market demands chemical.
Preparation of SOPS
To lay down a procedure for the preparation, approval, authorization, control and revision of Standard Operating Procedures.
Establishing documented evidence that provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specificatios and quality attributes.
Lab Equipments Validation
– HPLC, GC, FTIR Stability Chamber Software – Enviro
– Laboratory Information Management System (LIMS) and Computer System.
– Application Software Validation