We offer Stability Testing to support all phases of Product Development.

Pre clinical Stability Testing, Phase 1 Stability Testing, Support to various products like pharmaceuticals, Phase II and Phase III Stability Testing, Late Development stability testing to support final specifications and shelf Life, Registration Stability for NDA/MAA filings, Marketed Product Stability to ensure commercial quality control, Stability Testing to support scale-up and Post approval changes in existing process.

Stabicon Life Sciences offers formulation and analytical development services for OTC, Nutraceutical and natural products in oral solid, liquid, and semi-solid forms for clients across the globe. Stabicon deals with reputed major Pharmaceuticals and FMCG MNC companies and various other customers worldwide.

Stabicon has highly experience team for product development with more than 100+ years of combined experience to design formulations as per ICH Q8, Q9, Q10 and expertise in designing formulations by using reverse engineering techniques with non - infringing formulations.

Analytical research and development laboratory at Stabicon offers analytical method development and validation of prescription, OTC, nutraceutical, herbal and hygiene formulations and products. The laboratory is equipped with stare of art sophisticated equipment which enable us to deliver robust and stability indicating methods. We are also capable of performing analytical method verification, transfers and cleaning method validation on various surfaces.

We offer reverse engineering of various pharmaceutical products to study innovator profile. We also are capable to perform various tests like assay, degradation profile, dissolution and residual solvent using HPLC and GC equipments and  various wet lab tests like titrations and gravimetric tests can also be performed.

Our Microbiological laboratory is modern and fully equipped to perform tests to support different types of programmes. The facilities are fully cGMP compliant and include a Class 100 Bio safety cabinet. Our range of testing capabilities includes the following:

Bio burden test and validation, Disinfectant validation, Microbial limit Test, Microbial limit Test (TAMC, TYMC, specified microorganism), Vitamin assay and validation, Preservative Efficacy Test, Preservative efficacy test / Antimicrobial effectiveness test (PET / AET) and validation.

We at Stabicon have a specialized team which spearheads our research for the development of market-specific products. Our development scientists possess substantial experience and expertise in the area of formulation & development and transfer of technology of developed products.

Stabicon works on various dosage forms and various areas of generic, OTC, Nutraceuticals and Herbals. Manufacturing support, validation support, manufacturing of FSSAI products, Ayush products, work with CMOs.