• Here formulation begins with a thorough review of authentic literature; development protocol and other respective document groundwork; followed by the extensive pre-formulation study for the molecule under consideration, to reflect on the potential challenges and organize the valuable solution beforehand.

  • Moreover, formulation development processes programmed through project management to avoid redundant time lapse. Furthermore, every project has the respective area under discussion, interlinked into the system.

  • Years of development experience across a wide range of difficult to formulate drugs

  • Flexible facilities and conditions capable of handling very small batch sizes as well as highly toxic compounds and controlled substances

  • Preformulation and drug characterization

  • Development capabilities include  Hygiene products, sterile parenteral and oral liquids, lyophilized products, and oral solid dose including immediate and sustained/modified release.