Regulatory Affairs Consulting - IRIS GLOBAL

Regulatory Affairs Consulting Iris Global

Pharmaceuticals, 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States, 1-10 Employees

irisgra.com

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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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  • 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States Headquarters: 4655 Sagewood Cir, Queen Creek, Arizona, 53158, United States
  • 2011 Date Founded: 2011
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $1 Million to $5 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC 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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