Global Regulatory, Quality, Clinical & Medical Affairs Consulting
Medical Device/IVD, Drug, Biologic & Combination Products
Global Regulatory, Quality, Clinical & Medical Affairs Consulting
Medical Device/IVD, Drug, Biologic & Combination Products
Which Industries Do We Support?
Medical Devices/IVDs, Drugs, Biologics & Combination Products
What Do We Specialize In?
Global Regulatory Affairs
Global Quality Compliance
Clinical Affairs Strategy
Clinical Trial Operations
Medical Affairs
Program/Project Management
Business Excellence
How Are We Different?
The “E” in Eriah Group represents:
Elite Team of Executive & Senior Level Experts
Expedited Development Cycles with Accelerated Regulatory Timeline
Expertise from Concept Phase to Commercialization
Extensive Global Government Relations & Resource Networks
Our team of executive and senior level regulatory affairs, quality compliance, clinical, and medical affairs professionals have 25+ years each of global experience in healthcare drugs, biologics, medical devices/IVDs, and combination products.
We understand your needs firsthand, as we have extensive experience working with firms of all sizes, from start-ups to large global firms.
Our full services cover the entire product life cycle from concept to commercialization.
These Global Services Include:
Regulatory Submission Strategy
Pre-Clinical Strategy
Clinical Study Design
Clinical Research Operations
Quality Compliance
Quality Audits
Post-Market Surveillance
Compliance Remediation
Our team supports you in every step of the development process and we help you ensure that your products stay safe and effective.
Our team will work with your firm to develop a comprehensive and interactive training program tailored to meet the specific needs of your organization.
Training programs can be on-site or web-based, and can cover all topics associated with global drugs, biologics, medical devices/IVDs, and combination products in the areas of regulatory, quality compliance, clinical, and medical affairs.
We have a proven track record of improving regulatory, quality, clinical and medical affairs compliance and performance.
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