DDReg Celebrates 16 Years of Enabling Access to Global Healthcare

July 2025 - DDReg, a global regulatory affairs and life sciences partner, marks a significant milestone, 16 years of empowering healthcare innovators with regulatory clarity, speed, and strategy. Since its inception in 2009, DDReg has grown from a focused regulatory consultancy into a trusted global partner delivering end-to-end solutions for the pharmaceutical, biotechnology, and medical device sectors.

Founded by Neeraj Pant and Neeti Pant with a clear mission, to simplify regulatory complexities and improve access to healthcare, DDReg has stayed true to its vision: guiding life sciences companies from molecule to market and beyond.

From Local Consultancy to Global Partner

Starting with a small team of dedicated regulatory experts in India, DDReg quickly gained recognition for its deep regulatory knowledge, client-centric approach, and delivery excellence. Over the years, the company has expanded its global footprint, supporting product registrations and compliance requirements across North America, Europe, Latin America, MENA, APAC, and CIS regions.

"Our philosophy at DDReg is built on precision, agility and Insight. We don't just do routine regulatory jobs, we shape pathways with foresight and scientific depth, empowering our partners to bring their product to market swiftly" says Neeraj Pant, Co-Founder & Director of DDReg.

Today, DDReg operates with a multi-functional team of regulatory professionals, pharmacovigilance experts, medical writers, clinical specialists, and technology professionals. Its services span the entire product lifecycle from development strategy and global dossier submissions to post-marketing surveillance and regulatory intelligence.

Enabling Innovation with Expertise

DDReg has contributed to the success of more than 2,000 regulatory submissions, across generics, new chemical entities (NCEs), biologics, biosimilars, combination products, and advanced therapy medicinal products (ATMPs). Whether it's navigating the FDA, EMA, CDSCO, SAHPRA, JFDA, or other regulatory authorities, DDReg has consistently delivered results for innovators, helping reduce time-to-market and maintain compliance throughout the lifecycle.

Its pharmacovigilance services have processed more than 40,000+ ICSRs, while its clinical regulatory team has facilitated submissions for pivotal trials, audits, and pre-approval inspections globally.

Technology Meets Science

In the past few years, DDReg has embraced digital transformation to offer smarter regulatory solutions, integrating automation, regulatory informatics, and AI-assisted document management to enhance accuracy, efficiency, and decision-making.

"We believe the future of regulatory science lies in harmonizing human expertise with technology," says Neeti Pant, Co-Founder of DDReg. "This belief has driven our investments in regulatory tech and innovation platforms."

Looking Ahead: A Partner for the Future

In 2025 and beyond, DDReg continues to evolve to meet the needs of a dynamic life sciences landscape. With increasing focus on ATMPs, digital therapeutics, global harmonization, and patient-centric regulations, the company is doubling down on its strategic advisory services, global presence, and technology-enablement offerings.

https://www.ddregpharma.com/company

DDReg also remains committed to fostering thought leadership, sustainability, and regulatory capacity building in emerging markets, helping not just its clients, but the broader healthcare ecosystem.

A Message of Gratitude

The 16-year milestone is as much a celebration of DDReg's journey as it is a tribute to the people behind it.

"We are deeply grateful to every client, partner, and DDReg team member past and present, who has shaped our story," says the leadership team. "Together, we've not only met regulatory milestones, but also enabled access to safe, effective, and innovative therapies around the world."

As DDReg steps into its 17th year, its purpose remains unchanged: enabling access, accelerating innovation, and elevating regulatory standards for a healthier world.

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DDReg Pharma Inc, 1201 North Market Street Suite 111, Wilmington, DE 19801 (US)

DDReg is a global life sciences consulting firm specializing in regulatory affairs, pharmacovigilance, and quality services, accelerating product registrations and ensuring compliance through smart RegTech and deep industry expertise.

This release was published on openPR.