Therapiva private limited is an API manufacturing organisation based in Hyderabad having state of art manufacturing facility in Pashamylaram industrial area. Therapiva offers entire services for API and intermediates development including Lab assessment, Process optimization, Scale-up, API synthesis, API commercial Manufacturing. Therapiva’s state-of-the-art facilities including Analytical facility helps us to handle complex API’s and Intermediates and highly potent materials at both developmental and commercial scale to cater excellent quality services to our clients. Therapiva’s competent and experienced API team with global experience capable to deliver the projects at agreed timelines to meet client expectations with unparalleled quality and cost. Our proactive project management system offers seamless communication for project updates to clients. Therapiva has globally compliant cGMP facilities. With proven chemistry expertise and experience, Therapiva offers contract research and development, manufacturing services of APIs and intermediates.

Therapiva supplies, cGMP intermediates and KSMs to global innovators. It is equipped with flexible, versatile and advanced infrastructure, tailored to fit any complex chemistry molecules churning out of Innovator’s development pipelines. The manufacturing facilities complies with all regulatory guidelines and requirements of current Good Manufacturing Practices (cGMP) and are successfully inspected/approved by health and regulatory agencies. Therapiva has a road map to upgrade the facility to US-FDA standards in a span of 24 months.

Key features of the facilities


Six production blocks

Six production blocks spread over an area of 7 acres, and a mini-plant for scaling up of new products.


Over 70 Reactors

Total reactor volume of approximately 292 KL, with over 70 reactors with a balance of Stainless steel and glass lined reactors.

Wide range of process parameters

Capable of handling broad spectrum of reactions and wide range of process parameters.

CGMP certified

The facility is CGMP certified, and plans to be certified by US FDA, EDQM, WHO, TGA (Australia) and PMDA (Japan).

ISO 9001:2015 certified

It is also WHO GMP approved and ISO 9001:2015 certified.

Manufacturing base

Manufacturing base typically consists of high value/ low volume and low value/ high volume products.

Reverse osmosis systems

A Zero discharge facility with biological treatment, multiple-effect evaporators and reverse osmosis systems.

3 Clean rooms

3 clean rooms (Class 100,000) with 70L, 500L and 2000L crystallizers

These features ensure an effective structural methodology at workplace which includes manufacturing of quality products, rational and effective use of available resources, minimization of waste along with good safety and hygiene standards.  Safety aspects have been given utmost importance, in all aspects including plant installation, equipment, systems and trained personnel to ensure smooth productivity.  Combination of a dedicated team and world class production techniques guarantee delivery of products to customers across the globe.