Stay on top of Global Regulatory Requirements
Navigate complex regulatory landscape
Navigating The Global Regulatory Landscape
ekaGRA helps you navigate increasingly complex and stringent global regulatory intelligence requirements while improving and standardizing processes across functions and geographies.
Our global regulatory experts, data science expertise and evidence-based consulting spans across the R&D value chain of Drugs / Medical Devices / Cosmetics / Nutraceuticals, including clinical trials, marketing authorization submissions and life cycle maintenance.
ekaGRA provides regulatory intelligence that supports product benchmarking. Get access to validated data and knowledge to implement relevant regulatory changes across the value chain of the product.
Custom reports are created and shared in a tabular manner, which will help your team in taking faster and compliant decisions.
three steps to success
We Will Help You Every Step Of your product life cycle
Bio-Pharma
Growing patient safety emphasis and new product classes, countries are constantly changing or introducing new regulations
Medical Devices
Except for few countries, med device regulations are hazy. Device regulatory decisions are decentralized and require dependable information
Nutraceuticals
Consumer Health requirements are more complex than BioPharma as its breadth is wide (OTC, food, cosmetics, and you name it..).
What do we do?
- Reulatory Intelligence
- Regulatory Information Management
- Reporting
- IDMP
- Publishing
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- Pharmaceuticals
- Biologics
- Medical Devices
- Nutraceuticals
- Chemicals
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