K-source has a strong product development, implementation and delivery system. At the core of the product development is the strength of K-source’s knowledge source, which has strong product architecture that lays the foundation for efficient product development.

K-source has customized and semi customized products relevant for various verticals especially in chemical and pharmaceuticals.

K-source’s Audit Management is a powerful auditing solution that helps organizations assess their state of compliance. K-source’s Audit Management provides all the tools that an organization needs to benchmark the performance against internal, industry and regulatory requirements. This Audit Management brings in more clarity into the effectiveness of organizational control mechanisms, so that an organization can take fast, decisive action to reduce risk and ensure global compliance and also ensures to quickly organize effective audit programs.

K-source’s CAPA Management is a tight system that allows users in any department to initiate a corrective and preventive action to address and resolve an issue pertaining to them. By facilitating an effective CAPA process, K-source’s CAPA Management helps to resolve issues quickly and ensures that the issues don’t recur again. Our CAPA Management helps you identify the occurrence of nonconformance’s, customer complaints, incidents, discrepancies, out-of-specifications or any other quality issue and helps you facilitate compliance with requirements for electronic signature, electronic records and software validation such as 21 CFR Part 11 from the FDA. K-source’s CAPA Management meets internal and industry standards and regulatory requirements including FDA, cGxP, ISO 9000, ISO 13485, ISO 14000, ISO 14971, and others.

K-source’s Document Management is a Web-based solution that helps customers to create, manage and share critical documents and best practices throughout your entire enterprise in a cost effective manner. K-source’s Document Management integrates document management into your value chain – ensuring fast, secure access to information. This Document Management provides creation, versioning, approval, change, training and review processes in a single tool.

K-source’s Laboratory Information Management System (LIMS) is meant for the management of samples, users, instruments, standards and other laboratory functions such as invoicing, plate management, as well as work flow automation

LIMS facilitates the whole process of information gathering, decision-making, and calculation, review and release out into the workplace and away from the office. The goal is to create a seamless organization where:

• Instruments used are integrated in the lab network; receive instructions and work lists from the LIMS and return finished results including raw data back to a central repository where the LIMS can update relevant information in the LIMS.
• Lab personnel will perform calculations, documentation and review results using online information from connected instruments, reference databases and other resources using electronic lab notebooks (ELN's) connected to the LIMS.
• Management can supervise the lab process, react to bottlenecks in workflow and ensure regulatory demands.
• External participants (department, company) can place work requests and follow up on progress, review results and print out analysis certificates and other documentation (perhaps even historically).

K-source believes in a sound product development strategy, which lays the foundation for successful product development, implementation and delivery ensuring optimum business profitability for the customer.