Empowering the GMP industry with innovative engineering, automation, and compliance services, Kashico ensures seamless project execution aligned with global standards.
Kashico Consulting Services LLP established in 2019, is committed to providing top-tier consulting services for the life sciences and biopharma industries. With expertise in engineering, digitization and process automation, Pharma 4.0, risk-based CQV, CSV, compliance and project management, we deliver end-to-end solutions that ensure adherence to global regulatory standards.
Knowledge
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Consistency
Opportunity
We offer tailored turnkey solutions to optimize operations, ensure compliance, and deliver seamless integration, helping clients achieve long-term sustainability and meet global standards.
With experience in the US and India, we've delivered projects globally, navigating diverse regulations to provide tailored solutions.
Our expertise in life sciences and food industries, with years of experience in pharmaceuticals and biotechnology, gives us a deep understanding of regulated environments.
We ensure global compliance with expertise in 21 CFR Part 11, EU Annex 11, and ISPE GAMP5, reducing risk and accelerating your path to market.
We offer solutions that improve efficiency, streamline workflows, and ensure compliance, leveraging data analytics and cost-effective strategies for long-term sustainability.
We provide turnkey solutions, from engineering design to project implementation, digitization, risk management, and compliance, ensuring seamless integration and results aligned with your objectives.
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We deliver tailored IT solutions for businesses of all sizes. Here are some examples of our work.
Our consulting process begins with a through assessment of your current IT infrastructure & workflows.
Perform a analysis of the client's existing IT systems.
Develop IT solutions based on the analysis phase.
Regularly communicate with our client to any concern.