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.

Our services

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.

Industries Served

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

Other features

BMS Validation System

BMS Validation System, Sauter, Honeywell, Siemens, Johnsons

Regulatory compliances Services

Contract Laboratory or commercial testing labs or third party testing labs are driven by their customer and market demands chemical


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

Clinical Research Software

– Clinical Trial application software, PE Access

– SAS, WIN Non Lin, Application Software Validation

Preparation of SOPS

To lay down a procedure for the preparation, approval, authorization, control and revision of Standard Operating Procedures.