FAQ
Q: Is Genohope a manufacturer or a trader?
A: Manufacturer.
Q: Does Genohope manufacture Active Pharmaceutical Ingredients(APIs) or Finished Dosage Forms(FDFs)?
A: Both APIs and FDFs can be customized, developed and manufactured.
Q: Does Genohope outsource APIs while Finished Dosage Forms(FDFs) contract manufacturing implemented?
A: It depends. If any API urgently required, not on the Genohope’s Medicine List, we tend to source the raw material under the recommendation or suggestion of our customer. Certainly, self-made APIs are always the priority for Genohope’s CDMO activity.
Q: Are the medicines only available on Genohope’s product list?
A: Absolutely not. Our R&D team enables us to deal with any medicine required.
Q: Are capsules, tablets, sprays and injections available when manufacturing?
A: Currently, only Injections are available.
Q: What are the filling containers?
A: Vials, Cartridges and PFS are available.
Q: Is Genohope certificated with Good Manufacturing Practice(GMP)?
A: Genohope has scheduled to be inspected as GMP by NMPA in the middle October 2023.
Expectedly , the company will be approved by the end of 2023.
Q: Does Genohope have any DMF Files?
A: Genohope will submit two drug files for registration in 2024. Some more will be submitted for DMF registration.