Quality Control

The maintenance of a quality management system is crucial to a laboratory for providing the correct test results every time.

  • Our QC is having the latest technology/competent
  • Maintaining the highest possible standards for Quality Control as we are working on UKMHRA approvals
  • Highly qualified staff
  • Machineries are procured from the most renowned companies
The product manufacturing in the facility has commenced since March 2010. The areas of various manufacturing sections are as follows:

At Verve Human Care Laboratories Quality management System, in accordance with WHO GMP standards requirements is established, documented, implemented, maintained and continually improved. Ensure that the product conforms to specified requirements. This includes the preparation & effective implementation of documented quality assurance procedures, which are in accordance with the current good manufacturing practice (cGMP) requirements.

Quality Policy

To manufacture and market pharmaceutical formulations of requisite standards to comply with customer needs, enhance customer satisfaction and continuously improve the effectiveness of the quality management system

This shall be achieved by implementing the practices in processes and systems, updating and conforming to applicable regulatory requirements, continuous and dynamic improvements in quality of products and services.

Focus on Customer Orientation

The management recognizes the importance of current and futuristic needs and expectations of the regulatory market. It is committed to provide the necessary infrastructure and support to satisfy these needs at all level.


A totally committed management to adopt latest quality norms in pharma industry and empower people to achieve the goals.

Quality Assurance

The QA provides from time to time the necessary technical guidance through seminars, training programs, discussions, meeting and audits. In this endover, they pull the latest information on technology and GMO to keep the personnel aware of the latest knowledge in the Pharmaceutical Technical Environment.

Quality Goal through Participation

The management strongly believes in the capabilities of every individual and that he could significantly contribute in building quality and upgrade quality standards. With this view in the mind the management regularly organize the training program.

Continual Improvement

This approach is supportive to quality management at various operational levels and there is a reward system for individuals at all level of workmen, staff and management to recognize their contribution in improvement of system, reduce operational problems and systematizing the functional effectiveness and efficacy. This is permanent objective of the plant..

Responsibility of the QA Function

To ensure that both the operations and control of these processes are effective, various criteria and methods are determined, e.g. evaluation of suppliers, methods of finding customer satisfaction etc. .

Responsibility for the quality of the products to ensure that they are fit for their in-tended use , comply with the requirements of the marketing authorization and do not place patients at risk due to inadequate safety, quality or efficacy.

To implement the Quality Management System, various system related processes such as internal audit, management review, corrective and preventive actions, training, and various other operation related processes are identified.