We, Rescisco Global Regulatory consultants, intended to offer quality and regulatory services to the manufacturers of medical devices including in-vitro diagnostic medical devices from conceptualization stage to marketing as per the requirements.
Who We Are
We Don't Just Navigate Regulations — We Master Them.
Rescisco Global Regulatory Consultants was founded on a single conviction: that medical device companies in India deserve world-class regulatory guidance — not generic compliance checklists, but intelligent, product-specific strategy built for the long term.
Headquartered in Hyderabad — India's pharmaceutical and life sciences capital — we operate at the intersection of deep scientific understanding and rigorous regulatory knowledge. Our team comprises regulatory scientists, quality engineers, clinical affairs specialists, documentation experts, and former industry professionals who have sat on both sides of the submission table.
We serve the full spectrum: seed-stage startups taking their first CDSCO step, established Indian manufacturers pursuing EU CE marking or FDA 510(k) clearance, and multinational corporations seeking in-country representation, SUGAM portal management, and post-market compliance support.
"Regulatory compliance is not a cost centre — it is a competitive advantage. Companies that build it right from the start launch faster, defend their position better, and sustain market presence longer."
— Rescisco Global, Core Belief
The Rescisco Difference
Speed Without Shortcuts
We reduce time-to-market by eliminating avoidable delays: incomplete files, wrong classifications, missed regulatory updates. Rigour delivered efficiently.