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FAQ's

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Pharma Pack Corp specializes in the development, manufacturing, and packaging of pharmaceutical, cosmetic, and dietary supplement products. We offer end-to-end solutions, from formulation and private label development to full-scale manufacturing under strict quality and regulatory standards.
We primarily serve the United States market, operating under FDA-oriented standards, while also supporting clients across LATAM and Europe.
Yes. We provide comprehensive private label solutions, including formulation development, sourcing, branding support, manufacturing, filling, labeling, and packaging.
We manufacture cosmetics, personal care products, dietary supplements, and select pharmaceutical-grade products, tailored to client specifications and regulatory requirements.

Yes, we have an FDA cGMP-certified supplement manufacturer facility. The good manufacturing practices (GMPs) we adhere to meet both World Health Organization (WHO) and European Union (EU) requirements as well.

Yes. Our operations follow FDA guidelines, cGMP standards, and internal quality systems designed to meet U.S. regulatory expectations.

Absolutely. All products undergo strict quality control testing, documentation review, and batch traceability to ensure safety, consistency, and compliance.
Yes. Our scientific and technical team supports clients from concept and formulation through pilot testing, validation, and market-ready production.

Yes, we offer regulatory and compliance assistance, including formulation documentation, ingredient compliance review, and labeling guidance. We also provide the necessary documents for regulatory registration in other countries.

Yes. Confidentiality is a core value. NDAs are standard, and all proprietary formulations and client data are strictly protected.
We collaborate with both emerging brands and established companies, offering scalable solutions aligned with each client’s growth stage.

Still have questions? Contact our team to discuss your project.