Documents and certificates
The technical and regulatory documentation your product needs to register, import and sell.
Last updated:
We validate and gather the documentation that backs your product's quality and enables its registration and import in Chile. This avoids rejections, delays and friction at customs or with the health authority, with support that understands ISP and Food Sanitary Regulation (RSA) requirements.
What we deliver
- CoA (Certificate of Analysis) per batch.
- GMP / BPM certificate for the plant.
- Technical sheets and MSDS for each product.
- Certificates of origin and supporting documentation for import.
Regulatory support
We support compliance with the Food Sanitary Regulation (RSA) and the ISP regulations applicable to supplements, cosmetics and medical devices. We check that specifications, labeling and documents are consistent with each other and with what each procedure requires.
What it is for
- Register your product with the relevant authority.
- Import raw materials or finished product without customs friction.
- Demonstrate traceability and quality to clients and distributors.
Documentation is prepared together with development and manufacturing, not as an isolated step at the end. Free initial evaluation and a reply within 24 to 48 business hours.
How we integrate it into your project
Documentation is not assembled at the end as an isolated step: we plan it together with development and manufacturing, so specifications, labeling and certificates are consistent with each other and with what each procedure requires. That reduces back-and-forth and speeds up registration and import.
We tell you from the start which documents your product needs based on its category and destination, and gather them as the project advances. If you import raw materials or finished product, we also prepare the supporting documentation so the customs step is smooth.
All under a single point of contact, so the regulatory side stops being a bottleneck in your launch.
Frequently asked questions about documents and certificates
We answer the most common questions about your product's documentation.
-
We gather and validate the documentation your product needs to register, import and sell:
- CoA (Certificate of Analysis) per batch.
- GMP / BPM certificate for the plant.
- Technical sheets and MSDS for each product.
- Certificates of origin and supporting documentation for import.
-
The partner network's certifications (GMP, HACCP, ISO, FDA Registered, Kosher, Halal, among others) are reviewed and validated case by case, based on the country, plant and product. For each project we confirm which certifications and documents apply before moving forward, rather than publishing general folios.
-
We support compliance with the Food Sanitary Regulation (RSA) and the ISP regulations applicable to supplements, cosmetics and medical devices. We check that specifications, labeling and documents are consistent with each other and with what each procedure requires.
-
From the start. Documentation is planned together with development and manufacturing, not as an isolated step at the end. That reduces back-and-forth and speeds up registration and import.
-
Yes. We prepare the supporting documentation so the customs step is smooth, for both raw materials and finished product. We tell you which documents you need based on the category and destination.
Need your product's documentation?
Tell us your case and we will give you a free evaluation within 24 to 48 business hours, with no commitment.
Request an evaluation