Quality Policy and Quality Management System (QMS)

Quality Policy and Quality Management System (QMS)
Quality Policy:

Chemveda Life Sciences firmly commits and strives to be a leading global level service provider in research and development for pharmaceutical, biotech, agrochemicals and veterinary sectors through its effective implementation of Quality Management Systems for unsurpassed customer satisfaction in line with global quality standards and in compliance of statutory requirements.

Quality Management System (QMS)

Chemveda believes that “Quality in a product or service is not what we put into it, it is what the client or customer gets out of it.” It also reflects on our commitment of an On Time In Full (OTIF) delivery.

Quality is an inevitable fragment of Chemveda’s DNA and is an independent function to ensure the unbiased decision-making and avoid any conflicts of interest.

QMS is a formalized system which consists of QA & QC components. It documents processes, procedures, and responsibilities for achieving quality policies and objectives. As we operate out of a global regulatory network these standards prove to be powerful tools for effective management of compliance, customer requirements, delivery and overall organizational objectives.

Chemveda life sciences’ quality management system is an ISO 9001:2015 certified system which provides a customer centric approach with superior leadership for engagement of qualified teams. The QMS team also ensures that the organization sticks to the principles of continual improvements to add value to the R&D initiatives of our clients and all the key stakeholders. Also, this system helps us in evidence-based decision making by providing traceability cues and parameters.

As a team, the committed top management and all the key representatives of the company conduct an MRM (Management Review Meetings) once in every four months to ensure that all operations and deliveries are in sync with our quality policy and guidelines.

Key Elements & Responsibilities of QMS:
  • SOPs/Guidelines
  • Change Management
  • Vendor Management
  • Product release
  • Non-Conformity Handling and Redressal
  • Corrective & Preventive Action
  • Internal Audits
  • QMS Trainings
  • Complaint Handling & Redressal

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