Technical Support FAQ

Global Compliance Center

Are these manuals updated for 2026 regulations?

Yes. All operation manuals and Technical Data Sheets (TDS) are reviewed annually to ensure full compliance with the latest EU MDR (2017/745) and US FDA requirements.

Can I request a customized OEM manual for our brand?

Absolutely. For contract manufacturing (OEM) partners, we provide tailored technical documentation including white-labeling, specific local language translations, and customized SOP instructions.

Do you provide biological validation reports?

Individual validation reports (ISO 10993, SAL 10⁻⁶, EO residue) are part of our premium documentation package. These can be requested through our integrated TDS download portal.

How do Kingphar standards align with USP/BP/EP?

Our manufacturing protocols are engineered to meet or exceed the pharmacological requirements of the United States (USP), British (BP), and European (EP) Pharmacopoeias.