Quality & Compliance
Documentation is partof the product.
[ 01 ] Our Approach
Careful sourcing, appropriate documentation.
Healthcare products are subject to different regulatory, documentation and quality requirements across markets. Stige works to source products from suppliers capable of providing documentation appropriate to the product and destination market.
Regulatory requirements differ between countries, so each enquiry is assessed based on the product, destination market and buyer requirements. Documentation expectations are discussed early — alongside specifications, pricing, MOQ and lead times — so there are no surprises later in the process.
[ 02 ] Documentation
Documentation may include, where applicable:
Where applicable — by product and destination market
Certificate of Analysis
GMP documentation
Product specifications
Manufacturing licences
Free Sale Certificates
Certificates of Origin
Technical documentation
Product registration support documents
Export documentation
Tell us which documents your market requires.
Include your certification and documentation requirements in your enquiry, and Stige will assess sourcing options against them.