FAQs
Frequently Asked Questions About Pharma & Medical Device Consultancy
Answers to the questions manufacturers most often ask before starting a pharma consultancy engagement, whether for a greenfield facility, brownfield expansion, or new product development.
We support pharmaceutical and medical device manufacturers setting up greenfield or brownfield production facilities, as well as new product development for medical devices — primarily across Maharashtra's MIDC and other industrial zones.
Our project consultancy is focused on facilities located in Maharashtra, particularly MIDC and other industrial zones. The companies we work with — Indian or international — can be based anywhere, provided the project itself is being set up in this region.
We coordinate and consult across the full project lifecycle — land identification, approvals, planning, and readiness — while physical execution is carried out by specialist implementation agencies, which we help you identify and coordinate with.
Our new product development consultancy supports classification, research, design, and manufacturing setup for a product you've already identified, guiding each step so it's grounded in the right regulatory and market context — the choice of which product to build stays with you.
Greenfield refers to setting up a new facility on undeveloped industrial land. Brownfield refers to expanding, modifying, or repurposing an existing facility. Suchigo Consulting supports both.
This varies significantly depending on the scale of the project, land status, and regulatory requirements — best discussed directly for your specific case.
Share your requirement through our contact page, and we'll schedule a discussion to understand your project's scope and next steps.
Still have a question?
Share your requirement, and we'll walk through the specifics of your project directly.