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DDReg is Exhibiting

DIA Global 2024

Let’s meet at DIA Global 2024!

Meet our Business Development team at the DIA Global conference in San Diego between 16th and 20th June to discuss clinical, regulatory, and pharmacovigilance solutions for your pharmaceutical products. Our expertise covers generics, OTCs, cosmetics, medical devices, biologics, biosimilars, vaccines, dietary supplements, and more.

DDReg Pharma

Your Go-To-Partner For Regulatory and Drug Safety Solutions

DDReg is thrilled to announce that it shall be present and exhibiting at the DIA Global Annual Meeting in San Diego. Having exhibited at previous DIA conferences, the last being DIA Global 2023 in Boston, DDReg looks forward to connecting with key decision makers of the Pharma industry and engaging in discussions that are paving the way of healthcare. This year, DIA Global Annual Meeting celebrates its 60th Anniversary, or 60 years of providing Pharmaceutical stakeholders & organizations with the platform to engage in visionary strategies for development and impactful collaborations to drive healthcare forward.

In line with DIA’s 13 tracks, DDReg looks forward to offering its support & services to provider organizations in the pharma industry with solutions for clinical safety & pharmacovigilance, clinical trials & clinical operations, data & technology, medical affairs & scientific communication, patient-focused drug development, translational delivery technologies & precision medicine, project management & strategic planning, R&D quality & compliance, regulatory including CMC & product quality, statistics and data science, value & access, and professional development. Meet us at booth # 1708!

Our Team

Meet our Business Development team at the BIO International Convention in San Diego to discuss your requirements
for clinical regulatory, regulatory affairs, clinical safety, medical writing, and pharmacovigilance.


Neeraj Pant

Director & Co-founder


Akshita Srivastava

Assistant Manager (Business Development)


Swadhin Sekhar Biswal

Assistant Manager (Business Development)

Our Services



Our regulatory services can help devise tailored strategies, provide technical processes and on-going support in
Due-Diligence, Gap Analysis, New Product Authorizations...

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We optimize safety databases and technical ability to deliver high-quality and reliable safety measures with minimal risk across ICSR Processing & Submission...

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Our robust infrastructure and management processes ensure that dossier conversion. eCTD management and paper submissions are conducted efficiently and adhere...

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We provide updated labeling and compliance packages, that assist in the development of Product Labeling, Artwork Review & Compliance and Claim Substantiation...

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Medical Writing

The highly experienced medico-writing team have developed procedures and templates to ensure the modules of CTD are detail-oriented and additionally...

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IPR Support

Our collaboration with patent attorneys, with more than 20 years of highly experience, enables effortless delivery of product launches, market authorizations...

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Get In Touch!

Don't hesitate to contact us