Timelines vary based on the complexity of the study. Routine analytical testing can be completed in 5-7 business days, while comprehensive formulation or animal studies may take 4-12 weeks. We provide a detailed schedule upon protocol approval.

Yes, our research facility operates in strict adherence to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines to ensure data integrity and regulatory acceptance.

Absolutely. Our team can assist in preparing the necessary technical documentation and reports required for dossier submissions to regulatory bodies like DCGI, FDA, and EMA.

Yes, we specialize in tailoring research protocols to meet specific client needs. Whether it's a novel drug delivery system or a unique toxicity study, we can design a protocol that fits your scientific goals.