DDReg pharma

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DDReg Pharma

News and Events

High Impact Manager Program

DDReg & Oktane HR – “High Impact Manager Program”

DDReg places a strong emphasis on continuously nurturing and expanding its leadership team to drive long-term organizational success. In line with this vision, DDReg was fortunate to have been supported by Oktane HR- a leadership and growth focussed consultancy that is dedicated to refining leadership capabilities and learning. Principal consultant, Mr. Sunil Bhardwaj, and Lead […]

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Regulatory Excellence

DDReg features in BioPharma Dive

End to end global regulatory services driven through technology-enabled solutions.DDReg featured in BioPharma Dive, a leading Pharmaceutical Industry publication that provides insight into emerging trends and news that are driving the Industry. Among these trends is outsourcing regulatory affairs that have brought substantial value to the business by saving cost & resources, de-risking other business

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DIA Europe

DDReg Exhibits at DIA Europe 2023 in Basel, Switzerland

The European Union has seen some major changes and advances in Regulatory & Healthcare Policies and strategies- a key one being the “Regulatory Science to 2025” strategy to enhance EMA’s engagement with regulatory science. The need for proactive participation in such initiatives is important to support the strengthening of regulatory systems and facilitate innovation in

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DIA Europe

We are exhibiting at DIA Europe 2023

We are exhibiting at DIA Europe 2023 Meet our experts at booth #59 to discuss your queries on market access strategies , Regulatory Intelligence, Regulatory Strategies, Feasibility Studies, Life Cycle Management. Run your regulatory processes with our technology enabled platforms that help generate better data, for faster market access, safety and efficacy of vital, life-altering

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Information Security Management System

DDReg receives the ISO 27001:2013 certification for Information Security Management System

Ever since the incorporation, it has been DDReg’s endeavor to provide high quality services to its customers. To achieve this, DDReg has been consistently and regularly working towards improving its quality standards. For more than 6 years now, we have been achieving the high-quality standards set up by ISO 9001:2015, through the global accreditation agency

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DDReg Foundation Day Celebrates

DDReg celebrates its 13th Foundation Day

On Friday 1st July 2022, DDReg Pharma wholeheartedly celebrated its 13th Foundation Day. Employees from the Gurgaon, Mumbai, and Hyderabad offices connected virtually to commemorate not only the grand occasion but also each other’s milestones and achievements. The day consisted of fun activities including interactive games and performances by employees such as singing, instruments, poetry,

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DDReg attends National Conference on Pharmacovigilance and Clinical Research 2022

DDReg attends National Conference on Pharmacovigilance and Clinical Research 2022- Chandigarh College of Pharmacy

Drug abuse has gradually become an increasing issue due to the use of non-medical prescription drugs. Thus, pharmacovigilance and drug safety has become an even more crucial aspect for ensuring patient safety by monitoring adverse drug reactions and evaluating the safe use of medicines. To do this, robust procedures must be established while keeping in

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CPhI North America conference

DDReg to participate in CPhI North America conference in Philadelphia from 17th-19th May, 2022

CPhI provides a networking platform for pharmaceutical industry leaders. As America accounts for approximately 40% of global pharmaceutical sales, CPhI North America is the ideal event that encourages pharmaceutical experts to interact with each other regarding innovation within the industry. The 3-day, in-person, conference will touch on a broad horizon of relevant topics including market

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ddregpharma silver sponors of the 7th gcc pharma summit 2022 in dubai and UAE

DDReg Pharma: Silver Sponsors of the 7th GCC Pharma Summit 2022, Dubai, UAE

The healthcare ecosystem is driven by several factors. Government vision, successful partnerships, modern legislation, and adoption of innovation are some of the most crucial ones from a regulation point of view. Regulatory affairs (RA) bridge the gap between regulatory authorities and market access for drugs allowing patient empowerment by increasing drug availability. With ever-changing laws,

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