Kevin is an Industrial Automation Solution Provider for the Life Sciences Industry. We are focused on providing Automation, Process & MES solutions to Life Science Industry across India.
We have addressed various applications in Formulations / API / Biotech / Sterile areas of the Life Sciences industry like.
SCADA systems for production lines including batch production equipment.
Kevin is also an authorized & Certified Systems Integrator for Rockwell Automation.
The automation group has continuously built on its experience to bring you most advanced systems and instrumentation technology available today, while providing seamless compatibility with existing plant and operations.
Kevin offers Turnkey Automation solutions compliant to 21CFR Part 11 requirements in pharmaceutical industry. We undertake complete turnkey projects from basic to detailed engineering, system architecture, procurement, supply, installation, commissioning and validation.
The company’s expertise in supporting a wide array of PLC and Software platforms including Rockwell Automation, Zenon, Omron, Siemens & many others, makes it easy for you to support your installations.
Our engineers are highly experienced in executing projects on various PLC platforms and in doing SCADA, PLC Control and Automation projects in various levels of the plant from machine to process Design, Supply, Installation, Commissioning of PLC Systems, Field Instruments, Control Valves and SCADA Systems.
Why Kevin ?
Kevin Technologies is a leader in Regulatory Compliance & Validation Consulting & Services. Kevin also happens to be the pioneer for Regulatory Compliance Services in India & the largest company that provides Software & other GAMP based validation consulting in India & abroad.
We have the knowledge and experience to help the customers assess and define their compliance and validationrequirements. Our portfolio of services encompasses the entire product life cycle and includes GAMP ComplianceServices, Software Testing & Validation and projects requiring the integrated services of both these services.
Our dedicated pharmaceutical and computer systems division are uniquely qualified to optimize any validationeffort by applying quality validation services and the most current technology.
Our knowledge and experience in the life Science Industry, along with in-depth understanding of GAMPguidelines provides added value for our clients.
Data integrity refers to maintaining and assuring the accuracy and consistency of data over its entire life-cycle and is a critical aspect to the design, implementation and usage of any system which stores, processes or retrieves data.
As per MHRA:
The extent to which all data are complete, consistent and accurate throughout the data lifecycle. From initial data generation and recording through processing (including transformation or migration), use, retention, archiving, retrieval and destruction.
As per USFDA
For the purposes of this guidance, Data Integrity refers to the completeness, consistency and accuracy of data.
Complete, consistent and accurate data should be attributable, legible, contemporaneously recorded, original or a true copy and accurate (ALCOA).
General Root Cause : Data Integrity
Risk Based Approach covering the critical portion of Data Integrity
Configuration of systems - GxP function wise
Our advance Automation and validation solution provide powerful tools to the life science indutries to amke smooth transition from conventional to morden automated system which generate, transfer, maintain and capture original legible DATA with accuracy, completeness and consistency.
Kevin, one of the charter sponsors for ISPE in India, is the largest company in India, providing consulting & services in the area of regulatory compliances. We are the pioneers of Validation services in India and we offer various services to major Pharmaceutical companies across the globe
Kevin has more than 14 years and thousands of systems in validation experience.Kevin has the knowledge and experience to help the customers assess and define their compliance and validation requirements. Our portfolio of services encompasses the entire product life cycle and includes GMP Compliance Services, Validation Services and projects requiring the integrated services of both these services.
Our dedicated pharmaceutical and computer systems division are uniquely qualified to optimize any validation effort by applying quality validation services and the most current technology.
Kevin is the only company providing below services