API Manufacturing
Active Pharmaceutical Ingre dient (API) is the biologically active component of a drug product (tablet, capsule, cream, injectable) that produces the intended effects.
Impurity Synthesis
Impurity profile studies play significant roles in active pharmaceutical ingredient (API) development, which are closely related to the quality, safety and efficacy of drug products.
Custom synthesis and process development
Contract manufacturing involves production of goods by firm, under the label of another firm.Contract manufacturers provide such service to several firms based on their own or consumers specifications.
Scale up studies for any given process
The goal of scale-up is to identify & develop a process that will successfully produce a desired product when manufactured at a commercial scale.
Process Optimization.
the process by which manufacturers look for ways to improve their manufacturing process. A product's or system's optimization can take place on several levels.
Scale-up production from a few kgs to tons
Scaling up production to deliver more quantity of the product. Delivering with the same quality and efficiency.
Regulatory documentation, including DMFs (CTD format)
We Regulatory give documentation of our products with Drug master file. DMF the set of series of information for an Active Pharmaceutical Ingredient (API) or Drug substance brought together in CTD format as per regulatory requirements.