IKReg is a global regulatory services provider, offering end-to-end solutions for the pharmaceutical industry. We specialize in Regulatory Affairs (covering finished dosage forms and drug substances), Pharmacovigilance, Quality Management, Submissions Management, Labeling Management, Regulatory Information Management, and Regulatory Intelligence.
With deep industry expertise and a commitment to innovation, we empower clients to efficiently and effectively navigate complex regulatory landscapes. From regulatory strategy to submissions and compliance, IKReg is your trusted partner in ensuring product success and patient safety.
IKReg has established strong relationships with leading regional regulators. Our successful partnerships with over 50 manufacturers, including numerous industry leaders, highlight our commitment to excellence and regulatory expertise.
Our Mission
At IKReg, our mission is to drive your success through expert regulatory and quality support. With over 22 years of experience and strong industry relationships, we are committed to ensuring compliance and facilitating access to advanced healthcare innovations.
At the core of IKReg is our unwavering commitment to quality. We strive to be recognized for excellence by delivering top-tier regulatory compliance consultation services. Customer satisfaction and continuous improvement remain central to everything we do, ensuring we meet and exceed the expectations of our valued clients.
Why Choose Us
- We have various teams of qualified and professional people through which your objectives will take be met very easily.
- We offer hassle free and smooth work so that everyone can get the desired report in shortest span of time.
- Rationalizing the concepts is a part of our working.
- We evaluate the market and all the ranges of products which are known approved.
- On countless bases we make the regulatory report.