Explore DDReg’s Global Expertise

Navigating Global Regulations with Precision & Expertise

DDReg has a wide-reaching global presence, offering country-specific Regulatory Affairs (RA) services and Pharmacovigilance (PV) services designed to meet various regulatory requirements. Our expertise covers everything from strategic dossier submissions to post-market surveillance, ensuring compliance with the latest regulations. We guide clients through the requirements of health authorities such as the FDA, EMA, MHRA, TGA, and SFDA, helping to streamline approvals and effectively manage product lifecycles.

Partner with DDReg to accelerate your market entry and maintain regulatory excellence worldwide.

country-specific (RA) and (PV) services for global market

Our Solutions

Regulatory Affairs

Regulatory Affairs

Our regulatory services help devise tailored strategies, provide technical processes, and offer ongoing support in Due-Diligence, Gap Analysis, New Product Authorizations, and more...

Pharmacovigilance

Pharmacovigilance

At DDReg, we optimize safety databases and harness cutting-edge technology to deliver reliable safety measures with minimal risk...

Clinical Trial Reg Services

Clinical Trial Reg Services

DDReg offers comprehensive support to streamline your clinical trial regulatory submission process...

Medical Writing

Medical Writing

At DDReg, our seasoned medico-writing team delivers comprehensive medical and scientific writing solutions. Our expert services encompass regulatory submissions...

IPR Support

IPR Support

Our collaboration with patent attorneys, boasting over 20 years of experience, enables the effortless delivery of product launches, market authorizations, and regulatory filings...

Regulatory Intelligence

Regulatory Intelligence

Our regulatory intel and strategic advisory services offer in-depth market analysis of regulatory frameworks and competitive landscapes.

GMP & Compliance

GMP & Compliance

Elevate Your Manufacturing Standards with DDReg’s Expert GMP Compliance Services. Good Manufacturing Practice (GMP) compliance is critical for ensuring the safety, efficacy, and quality of pharmaceutical and biotechnology products.

Toxicology

Toxicology

Empower your regulatory journey with DDReg’s Toxicology Solutions. DDReg offers a broad spectrum of toxicology and risk assessment solutions designed to address complex safety and compliance challenges.