Bring your formulations from lab bench to global markets with a single, integrated pharma regulatory partner. We support you across the full Indian and export lifecycle—test licences (CT-12/13, CT-16/17), manufacturing licences (CT-21/23), import registration (Form 40/41), import licences (Form 9/10), and drug licences (Form 20B/21B)—so your products clear every gate with clean documentation and clear timelines.
Beyond approvals, we unlock growth with Export NOCs, Dual-Use NOCs, Written Confirmations, Neutral Code allocation, eCTD-ready dossier preparation, BA/BE and toxicity study coordination, and Free Sales Certificates, giving you a complete evidence and permissions stack for regulators and buyers in India and abroad.