About Us
What Do We Specialize In?
Global Regulatory Affairs & Quality Compliance
Global Clinical Strategy & Development
Medical Affairs
Project Management
Which Industries Do We Support?
Drug, Biologic & Medical Device Industries & Related Industries
How Are We Different?
(Here are Some of the Secrets Behind the “E” in Eriah Group)
Elite Team of Executive & Senior Level Experts
Extensive Global Government Relations & Resource Networks
Expertise from Concept Phase to Commercialization
Expedited Development Cycles with Accelerated Regulatory Timeline
Leadership
Our team of executive and senior level regulatory affairs, quality compliance, clinical, and medical affairs professionals have an average of 25+ years each of global experience in the healthcare drug, biologic, medical device and combination product industries.
We understand your needs first-hand as we have extensive experience working with all sized firms from start-ups to mid and large size firms.
Services at a Glance
Global Regulatory Affairs
Global Quality Compliance
Global Clinical Strategy & Development
Medical Affairs
Inspection Readiness, Responses & Remediation
FDA U.S. Agent & FDA Official Correspondent
Regulatory, Quality & Clinical Pre- & Post-Acquisition and Pre-Divestiture Support
Program Management & Business Excellence
Training
Training
Our team will work with your firm to develop a comprehensive and interactive training program tailored to meet the specific needs of your organization.
Our training programs can be on-site or web-based and can cover all topics associated with global drug, biologic, medical device and combination products in the areas of regulatory, quality compliance, clinical, and medical affairs.
We have a proven track record to transfer the skills and knowledge necessary to improve regulatory, quality, clinical, and medical affairs compliance and performance within your firm.