About Us

Company Profile

Established in 2007, Tirupati Group is a highly respected name as a fully integrated Indian Contract Manufacturing Company located amidst the green fields of Himachal Pradesh and are leading global providers in Pharmaceuticals, Nutraceuticals and Ayurvedic Formulations. Owing to persistent values of customer satisfaction, unsurpassed quality standards, human safety, innovation, etc. the company can boast of, a turnover that counts more than 500 Crore INR and serves a clientele of more than 40 reputed companies.

Employing a team of more than 450 highly skilled and experienced personnel for product testing, Tirupati Group has its own DISR approved Research and Development centre accompanied by a Pilot facility; to serve pre-formulation, formulation, analytical development, stability & scale-up services for all segments. Our portfolio of products includes Solid, Semi-solid, Liquid and Powder Dosage forms and is spread over more than 15 acres of land with which Tirupati Group is able to meet the domestic & international requirements.

With this objective blend of young dynamism and a visionary perspective, the company has been inexorably widening their spectrum of clientele continually.

Quality Policy

Tirupati Group is committed to providing paramount consumer satisfaction through quality and timely delivery. We are dedicated to successful collaboration with internal and external customers to ensure integration of best practices and quality processes that are developed, maintained and improved continually.

We strive to identify, meet and exceed our customer’s quality requirements through good manufacturing practices. We follow regularly updated methods for evaluation of the safety, efficacy, identity, strength and purity of our products, while facilitating innovation and improvement thereby adding value to our customers.

Our Quality Policy is based on the following principles :
  • Technical Know-how and Execution : All the processes are implementedas per the SOP (Standard Operating Procedures) and internationally certified manufacturing standards.
  • cGMP : All the processes and activities are in total compliance with cGMP principles.
  • Authentication of Documents : Retrieval, validation, and verification of data and documents of our processes and products; is guaranteed at all times due to organized compilation and preservation.

We are pledged to the compliance of all requirements as prescribed by national and international regulations. We firmly believe that our key to success is our QMS (Quality Management System) based on the cGMP requirements that ensure effective controls applied to our work processes.