frequently askedquestions

Glass2med, Lda materials are available in a range of standard digital formats, depending on the product and intended use. Common options include PDF for documentation, web-ready files (e.g., HTML), and editable source formats where applicable. If you have a specific workflow requirement, please contact our team and we will confirm the best available format for your needs.

Yes. Glass2med, Lda supports custom R&D projects through collaborative engagements tailored to your technical requirements, timelines, and regulatory constraints. Share your objectives, target application, and any existing data, and our team will propose a scope, milestones, and deliverables for review.

Glass2med, Lda operates under a documented Quality Management System (QMS) aligned with applicable medical device regulatory requirements. We maintain controlled procedures for risk management, supplier oversight, production controls, change management, and post-market activities to support consistent product quality and compliance.

Yes. Glass2med, Lda provides technical documentation and product characterization upon request. Depending on the item, this can include datasheets, drawings/specifications, traceability information, and available characterization results (e.g., key physical and optical properties) to support evaluation and integration.