Regulatory Affairs Consulting Iris Global
Pharmaceuticals, 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States, 1-10 Employees
Who is 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 a...
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- Headquarters: 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States
- Date Founded: 2011
- Employees: 1-10
- Revenue: $1 Million to $5 Million
- Active Tech Stack: See technologies
Industry: Pharmaceuticals
SIC Code: 8742 | NAICS Code: 237210 | Show More
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Frequently Asked Questions Regarding Regulatory Affairs Consulting - IRIS GLOBAL
Answer: Regulatory Affairs Consulting - IRIS GLOBAL's headquarters are located at 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States
Answer: Regulatory Affairs Consulting - IRIS GLOBAL's official website is https://irisgra.com
Answer: Regulatory Affairs Consulting - IRIS GLOBAL's revenue is $1 Million to $5 Million
Answer: Regulatory Affairs Consulting - IRIS GLOBAL's SIC: 8742
Answer: Regulatory Affairs Consulting - IRIS GLOBAL's NAICS: 237210
Answer: Regulatory Affairs Consulting - IRIS GLOBAL has 1-10 employees
Answer: Regulatory Affairs Consulting - IRIS GLOBAL is in Pharmaceuticals
Answer: Regulatory Affairs Consulting - IRIS GLOBAL contact info: Phone number: Website: https://irisgra.com
Answer: 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 submissions 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.
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