Drug Development Management
and Regulatory Services

RRI Group is a Full Service Global Regulatory and Management Company that collaborates with pharmaceutical, device, and biotech companies in the development of novel branded and generic therapeutics and devices.
About RRI Group
RRI Group is a Full Service Global Regulatory and Management Company.

RRI group collaborates with pharmaceutical, device, and biotech companies in the development of novel branded and generic therapeutics and devices.

RRI Group specializes in 505(b)(2) NDA / ANDA submissions, and 510K projects. RRI Group, Inc. helps clients obtain FDA approvals by delivering high quality regulatory and clinical strategies, solutions and services, with the demonstrated ability to save our clients time and money.

RRI Group’s our proven track record and experienced staff, manage clinical trials across the globe. RRI Group’s global relationships with clinical partners place us in an excellent position to execute your clinical program with efficiency and in a cost effective manner.

RRI Group services include the full spectrum of program management; regulatory, clinical endpoint studies, bioequivalence (in healthy volunteer and patient populations), data management, and compliance and audit (GMP, GLP, GCP) services. RRI Group leverages its access to renowned researchers, regulatory personnel, and facilities, in North America, Europe, Oceania, and Asia, to achieve unparalleled scientific, clinical, and business results while reducing the time of development and approval that significantly lowers the costs to our clients.

RRI Group is headquartered in Lake Wylie, SC, near Charlotte, NC, and has regional offices and associates across the globe. Our passion is Helping Companies…GROW!


We invite you to contact us about your drug development needs, as well as our cGMP, cGCP and cGLP inspections and auditing services. We can build a foundation for your product development needs.



Product Marketing Opportunities

Regulatory / Project Management

Clinical Project Management

Submission Preparation

Audits

Technology Transfer



We invite you to contact us about your clinical trials, drug development needs, as well as our cGMP, cGCP and cGLP inspections and auditing services. We can build a foundation for your product development needs.
RRI Group…Helping Companies GROW!

info@rriint.com
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