Manufacturing

Our medicines are made at two sites in Telangana, India. Both are designed and operated to EU-GMP and US FDA standards.

Exterior view of the Jadcherla facility, Telangana
Jadcherla, Telangana
Exterior view of the Jeedimetla facility, Telangana
Jeedimetla, Telangana

Jadcherla

Established
2014
Location
Green Industrial Park, Jadcherla, Telangana
Site area
444,300 sq ft
Capabilities
Cytotoxic oral solid dosages and sterile injectables; biopharmaceutical API and sterile injectables in lyophilised vials and pre-filled syringes; hormones and critical care products in oral, semi-solid and sterile injectable forms

Jeedimetla

Established
1979
Location
Jeedimetla Industrial Area, Telangana
Site area
43,500 sq ft, with 30,000 sq ft constructed
Capabilities
Cytotoxic oral solid dosages; sterile injectable formulations

Quality

We are committed to delivering safe, effective and reliable medicines. That commitment rests on a quality management system, and on a culture where every colleague is accountable for product quality and patient safety.

Regulatory compliance
We work in full compliance with the quality regulations, codes and standards that apply to us.
Defined procedures
Our procedures set clear expectations for any work that affects product quality, product registration, or the data supporting it.
Competency and training
Everyone working for us is given the education, training and experience to do their role properly.
Data integrity
Records, documentation and data are managed in line with applicable requirements.
Issue escalation
Established processes escalate anything that could affect product integrity or patient safety.
Third-party oversight
We hold third parties working on our behalf to the same standards we hold ourselves to.

We monitor and review our performance against this policy, and we expect it to keep improving.

What we make