Yes. All of our pharmaceutical ingredients and packaging components are sourced from FDA-registered, GMP-certified facilities. We ensure full compliance with relevant regulatory frameworks, including FDA 21 CFR, USP standards, ISO certifications, and, where applicable, FDA 510(k) clearance.
Yes. Certificates of Analysis (COAs), Safety Data Sheets (SDSs), and technical specifications are available for all products. Drug Master File (DMF) information can be provided for registered APIs upon request and under appropriate confidentiality agreements.
For in-stock products, orders are typically processed and shipped within 3–5 business days. International or made-to-order items may vary based on sourcing origin and regulatory review. We offer flexible shipping options, including temperature-controlled logistics for cold chain products.
Yes. We offer private labeling, custom packaging kits (e.g., vial/stopper/seal sets), and equipment solutions tailored to your specific operational or branding requirements.
Our clients include hospitals, pharmaceutical manufacturers, diagnostic labs, clinical research organizations (CROs), and third-party logistics providers (3PLs). We understand the unique regulatory and operational needs of each sector.
We implement rigorous quality assurance processes, including supplier qualification, batch-level documentation, and serialized tracking where applicable. All products are inspected and verified prior to dispatch.
Yes. We understand the need for evaluation before full-scale procurement. Samples or small-batch orders can be arranged for most product categories, subject to availability and regulatory status.
Our technical support team includes regulatory specialists and product engineers. You may contact us at info@unitechsupply.com, and we will direct your inquiry to the appropriate expert.
