Research at Ciro Pharma includes both generic and complex pharmaceuticals.
Having expertise in developing drug products having poor solubility and requiring solubility enhancement and bio-availability enhancement is the critical component of Ciro Pharma.
The formulation R&D helmed by top-notch experts is adept at developing regular generics as well as innovative products for Global requirements.
We have full capabilities to handle development services for a variety of dosage forms including:
Tablets, capsules and powders
Pellets and beads
Parental Dosage Forms (Liquid and Lyophilized powders)
Granules for reconstitution
Drug in capsule/vial for clinical trials
Analytical Method Development for Drug Products.
Analytical Method Verification for Drug products.
Analytical Method Validation for Drug Products.
Analytical Method Transfer for Drug Products.
Stability studies of formulations in accordance with applicable guidelines.
Preparing complete specifications for raw materials, APIs, and Finished products.
Cleaning validation & Detoxification studies.
Pre-formulation studies, Physico-Chemical Characterization and Reverse Engineering.