| • |
Formulation development technology |
| • |
Providing layouts for manufacturing facilities
for non-sterile as well as sterile preparations, keeping in
view international as well as Schedule M requirements for
GMP compliance |
| • |
Supervision of erection of facilities
to ensure compliance with plans and regulatory requirements |
| • |
Consultancy for identifying equipment for
manufacturing pharmaceutical products |
| • |
Quality management systems, including setting
up QC laboratories |
| • |
Product development technology |
| • |
Preparing regulatory dossiers for obtaining
various licenses from central as well as state licensing authorities |
| • |
Stability studies |
