


Regulatory Affairs Consulting - IRIS GLOBAL Email Formats
Pharmaceutical Manufacturing • Queen Creek, Arizona, United States • 1-10 Employees
Regulatory Affairs Consulting - IRIS GLOBAL Email Formats
Regulatory Affairs Consulting - IRIS GLOBAL uses 2 email formats. The most common is {last name}{last name} (e.g., doedoe@irisgra.com), used 75% of the time.
| Format | Example | Percentage |
|---|---|---|
{last name}{last name} | doedoe@irisgra.com | 75% |
{first initial}{last name} | jdoe@irisgra.com | 25% |
Key Contact at Regulatory Affairs Consulting - IRIS GLOBAL
Strategic Regulator Raexpert
Director Consulting Partner, Expert In Regulatory Affairs And New Business
Company overview
| Headquarters | 21371 S 185th Way, Queen Creek, Arizona 85142, US |
| Phone number | +12244336063 |
| Websites | |
| NAICS | 3254 |
| SIC | 611 |
| Keywords | Distribution, Pharmaceutical, Medical Device, Business Development, Gmp Audits, Strategic Regulatory Consulting, Costmetics, Nutritionals, Consulting - Latin America Regulatory Affairs, Dossier Review, Support With Local Health Authorities (Meetings), Preparation And Submission, Provide Temporary Regulatory Country Resources |
| Founded | 2011 |
| Employees | 1-10 |
| Socials |
About Regulatory Affairs Consulting - IRIS GLOBAL
IRIS Global is a consulting firm that specializes in and understands the regulatory environment across Latin America and the Caribbean. Just as important, we also understand the culture and business practices that are required to be successful, from the smallest island to the powerhouse of Brazil. We work and support companies who: • Would like to enter or expand into a Latin American or ROW • Struggle with incomplete or poor regulatory filings causing products to lose marketing authorizations (market share) • Feel that the regulations are constantly changing, causing rework and delays • Cannot find the skilled and experienced resources to keep up with the regulatory demands. • Have a regulatory team focused on the U.S., Europe or Asia but do not have a team that fully understands Latin America We can answer your regulatory questions and/or act as your regulatory affairs group for a specific country or for the entire region. We can prepare your product dossiers, file in-country, respond to health authority questions and monitor a submission’s progress through approval. With our team in the U.S. and our specialists in major countries, we offer a full set of capabilities that are normally only available to the largest companies.
Employees by Management Level
Total employees: 1-10
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Regulatory Affairs Consulting - IRIS GLOBAL has 5 employees across 2 departments.
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Regulatory Affairs Consulting - IRIS GLOBAL has never raised funding before.
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