Regulatory Affairs Consulting - IRIS GLOBAL LLC

www.irisgra.com

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.

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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.

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Country

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State

Arizona

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City (Headquarters)

Queen Creek

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Employees

1-10

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Founded

2011

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Estimated Revenue

$1 to $1,000,000

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Potential Decision Makers

  • President

    Email ****** @****.com
    Phone (***) ****-****
  • President Regulatory Affairs

    Email ****** @****.com
    Phone (***) ****-****
  • Dir. Reg Affairs and Quality and Pharmacovigilance Latam

    Email ****** @****.com
    Phone (***) ****-****

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