Subtle analytical lab is well equipped with all the necessary instruments/equipment’s that are mandatory to carry out especially Method Development & Validation activities that lead to characterization and profiling of products with a young and passionate team which can be leveraged to suit the requirements.
Analytical Method Development and Method Validation studies are performed/complies as per ICH and regulatory guidelines. Developmental studies at subtle can also be carried out as per customer’s/vendor/client requirement in accordance with their specifications. Stringent cGMP (current Good Manufacturing Practice) and GLP (Good Laboratory Practice) regulations are followed in Subtle Pharma.
Subtle has Enriched with Experienced Scientist’s to Identify, Isolate and Characterize the unknown impurities with advanced techniques.
We will provide Analytical Testing Services for various types of Pharmaceuticals, API’s/Raw-materials, Excipients, Intermediates, Phytochemicals, Agrochemicals, Pesticides, Nutraceuticals and Dietary Supplements, but not limited to. Analytical Services like FT-IR, HPLC, LC-MS/MS, NMR, TGA, Preparative HPLC and GC are also offered by Subtle Pharma.
Accelerated and Real time stability studies at cGMP environment of Pharmaceutical products are feasible along with Chemical, Thermal and Photochemical forced degradation studies at Subtle Pharma.
In order to verify the shelf life and storage conditions of a Pharmaceutical products, excursion studies are performed with Light, Temperature and Humidity