
FAQ
Frequently asked questions
- 01
Absolutely. We supply all necessary documentation, including Certificates of Analysis (CoA), Material Safety Data Sheets (MSDS), and regulatory filings to support your compliance requirements.
- 02
Yes, all our APIs comply with applicable United States Pharmacopeia (USP) or National Formulary (NF) monograph standards, ensuring the highest quality and safety.
- 03
We offer a comprehensive catalog of over 1,000 FDA-registered APIs, including analgesics, antibiotics, antifungals, vitamins, and more, catering to diverse pharmaceutical manufacturing needs.
- 04
Yes, through our partnerships with cGMP manufacturers and ISO-certified laboratories, we can assist in sourcing or developing custom APIs tailored to your specific needs.
- 05
You can reach out to our sales department via email or phone, or fill out the inquiry form on our website. Our team will respond promptly to assist you.
- 06
We offer competitive pricing and flexible payment terms. Please contact our sales team for detailed information tailored to your order and partnership requirements.
- 07
We maintain stringent quality control measures, including thorough testing and validation processes, to ensure the purity and efficacy of our products.
- 08
Yes, we can provide samples of our APIs for your testing and evaluation purposes upon request.
- 09
We coordinate with reliable logistics partners to ensure timely and safe delivery of your orders, adhering to all regulatory requirements for pharmaceutical products.
- 10
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