Since its establishment TIME Pharmaceuticals has always committed to achieve excellence in Quality Standard. Every product manufactured and distributed by TIME Pharmaceuticals with international guidelines of cGMP. Every unit has a well defined Standard of Procedure (SOP) and systems in place in compliance with the requirements of the Current Good Manufacturing Practices (cGMP), WHO.

The company achieves its objective of high Quality Standard by procuring raw materials from highly reputed international suppliers committed to internationally accepted cGMP guidelines. 


  • Enhance product quality by adopting latest technologies, equipments and use of quality ingredients

  • Continuously monitoring the manufacturing system in order to deliver, assured quality before distribution and sales

  • Continuous training and motivation, to personnel's for effective implementation of quality systems.

  • Enhance the customer satisfaction by analyzing the customer complaints and feedback regularly.



We have state-of-the-art infrastructure to manufacture products of world-class quality, conforming to national & international standards.

TIME Pharmaceuticals Quality Assurance department monitors and ensures implementation of Quality Policy and Quality management system in all pharmaceutical operations.

TIME Pharmaceuticals Quality Assurance System is guided by Quality Policy and Quality Manual. All pharmaceutical activities are organized and implemented according to the current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP).

Regular training program is conducted as per the annual training calendar and training needs identification. All employees are encouraged for regular up-gradation of their technical knowledge through regular knowledge-sharing training and discussions.  

The tools for Quality Risk Management are applied to different aspects of Pharmaceutical quality as per ICH Q9 guidelines.