08 — FAQ
Questions? Answered by our pharmacists.
For medical information, quality complaints or business development, contact us below. For urgent adverse events, use our 24/7 pharmacovigilance line listed in contacts.
What does SincoPharm produce?
Prescription medicines (Rx), biologics, vaccines, OTC and hospital injectables across oncology, immunology, CNS, cardio-metabolic, anti-infectives and rare diseases.
Are SincoPharm facilities GMP certified?
Yes. All commercial sites are EU GMP and FDA cGMP compliant, with WHO prequalification for vaccines and essential medicines. Audit reports available to partners under CDA.
How can I become a distributor?
Send your company profile, licenses, cold-chain capabilities and target portfolio via the contact form. Our alliance team replies within 3 business days.
Do you offer CDMO services?
Yes — from development to commercial: formulation, analytical, sterile fill-finish, lyophilization, biologics DS/DP and packaging with full regulatory support.
Where are clinical trial results published?
On registries and in our newsroom. We commit to publish all Phase II-III results regardless of outcome within 12 months of last patient last visit.
How do I report a side effect?
Use the contact form with subject “Pharmacovigilance” or call our 24/7 safety line. Provide product, batch, and contact for follow-up. We handle all reports per GVP.
