USA
India
Germany
SingaporeWe help our life sciences customers in accelerating their revenue growth by driving fast track registrations in global markets and maintaining regulatory compliance through the life of their products. With the right blend of experience, relationships, skill, innovation and in-depth expertise in pharmaceutical regulatory affairs, we bring top quality regulatory services to our clients
"Ensure quality, speed to market and compliance to our customers with strong regulatory practice propelled by process automation using latest technology"
To be among top 10 global pharma service organization by year 2030
Take a look at why DDReg is the preferred regulatory and drug safety consulting firm for top pharmaceutical companies
Robust regulatory strategies based on market intelligence, regulatory subject matter expert network, on ground experience in over 35 countries
Partner with our customers to run regulatory strategy (pre-registration) to life cycle management processes for product portfolios
Drug Regulatory compliance obligations like submissions, queries resolution, license tracking, pharmacovigilance and regulatory interactions
High quality submissions with speed through automated processes and proprietary regulatory metadata libraries and tools
Our domain expertise, technical competence, along with strong values is why leading global
pharmaceutical organizations prefer DDReg as their valued partner
To continuously meet the quality levels expected by our customers
Integrity at all times in the business decisions and the manner in which we conduct
Business
Excellence is not only a value but a means for doing the business
Striving for excellence with spirit of teamwork
Practice openness & encourage a sense of doing what's right through open communications
Committed to deliver high quality services
