Full Support for Pharmacopeia, GLP/GMP, FDA 21 CFR Part 11 and Other Regulations

Ignitive Lims Compliant with IP, BP, USP, EP, and JP

Ignitive lims is supportive for those stipulated in the Indian Pharmacopoeia (IP), British Pharmacopoeia (BP), United States Pharmacopeia (USP),European Pharmacopoeia (EP) and Japanese Pharmacopoeia (JP). Naturally, the software is also compliant with the specifications required by each Pharmacopeia. In addition, the check conditions can be saved. As a result, once the conditions are saved, checks can be performed easily just by calling them up as needed. Check results can also be saved.

Software Features of Ignitive lims for the Pharma Industry

Quality control is of utmost importance at any stage of production of medicinal products for human and veterinary use. The pharmaceutical industry takes care of that fact with concise, elaborate and meticulously described instructions – but regional regulations vary. The software of ignitive lims for the determination of density, viscosity, optical rotation, extraction, refractive index, turbidity, and temperature complies with worldwide requirements