Regulatory Services in Panama

Overview

Being a gateway to enter Central America and the Caribbean, Panama (República de Panamá) attracts foreign medicinal products and medical device investments. Ministerio de Salud de la República de Panamá (MINSA) overlooks the registrations, licensing and product approvals for the region. Even though the region offers good business opportunities, navigating the Panama’s regulatory regime requires a complete know-how on the procedural challenges.

With an expert Regulatory affairs team tracking down the regional regulations in a continuous fashion, Freyr assists foreign pharmaceutical manufacturers to enter the region successfully.

Freyr Offerings

Strategic Regulatory Consulting
Regulatory Affairs & Regulatory intelligence
Product registration

Freyr Advantages

Proven Regulatory affairs expertise
End-to-end Regulatory consultation
Structured and cost-effective approach to ensure speed to market
Shorter turnaround times

Creating compliant packaging for a cosmetic product is a collaborative effort of various departments in an organization such as: Labeling, Artwork and Regulatory Affairs. While label artwork must be validated by an artwork labeling team, it must combinedly be reviewed and approved by Regulatory Affairs team to ensure the compliance.

Artwork services for the current Consumer Healthcare/Food Supplements landscapes are divided as per the markets. For Compliance based markets, artworks are created by Freyr team and submitted to the client for finalizing the artwork/ label.

The current medical device landscape has turned challenging for manufacturers in terms of ensuring quality and audit compliance due to ever-evolving regulations which may lead to extended time for approvals and market access.

Overview

Freyr Offerings

Freyr Advantages

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