We, Bio-Innova & Synchron, has developed and validated methods according to US-FDA guidelines for various drugs using high technology and validated equipments. Our modern bio-analytical facility, operated by expert scientists, is complied with the Good Laboratory Practice (GLP) and ISO/IEC 17025 requirements. Our hardware and software are 21 CFR Part 11 compliance.

List of laboratory equipments (attachment)
List of developed and validated bioanalytical methods (attachment)