Regulatory consulting and compliance platform for pharma approvals
DDReg Pharma operates a regulatory consulting practice backed by proprietary AI tools (Regulatory Intelligence Platform, RIMS) for pharmaceutical and biotech companies navigating global approvals. The hiring profile is heavily weighted toward senior legal and regulatory talent (14 of 17 open roles), concentrated in India, suggesting a scaling model built on domain expertise rather than product engineering — a contrast to tech-first regulatory software.
Founded in 2009 and based in Gurgaon, DDReg Pharma provides specialized regulatory consulting across pharmaceuticals, biologics, medical devices, and food sectors. Core services span Regulatory Affairs, Pharmacovigilance, Quality, GMP Compliance, IPR, and Toxicology, with typical engagements covering product registration acceleration, CMC strategy, CTD dossier compilation, and post-market compliance. The business operates across major markets including Africa, GCC, LATAM, and ASEAN, serving companies from early development through commercial lifecycle.
DDReg Pharma currently hires exclusively in India, with 17 active roles across regulatory, legal, healthcare, marketing, and product functions.
DDReg uses Adobe Creative Suite (Photoshop, Illustrator, Premiere, After Effects), Microsoft Office stack, Sales Navigator, Apollo.io, HubSpot, Mailchimp, and Google Analytics — primarily commercial SaaS and content creation tools rather than proprietary engineering infrastructure.
Active projects include CTD dossier compilation and preparation, CMC regulatory strategy and gap analysis, marketing authorization applications across AFRICAS/GCC/LATAM/ASEAN, and remediation of deficiencies in regulatory submissions.
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