Analytical Development
- Method development & validations for API and finished product.
- Testing of API, excipient(s) and drug product
- Method transfer to manufacturing site.
Our Analytical Development Services team has the competence to develop and validate laboratory methodologies for new and generic pharmaceutical products to monitor ongoing stability and support the formulation and manufacturing process from development to commercialization. This in-house activity utilizes modern equipment such as Dissolution Test App. (14 stn), UPLC, HPLC, FTIR, UV/VIS, GC
with HS, Laser Particle Sizer, Osmometer, Liquid Particle Counter.
