Regulatory ServicesIn Indonesia, imported pharmaceuticals and medical devices must be registered with Indonesia's National Agency of Drug and Food Control (BPOM) before being distributed. The foreign pharmaceutical manufacturer must have its own subsidiary, manufacturing facility, or authorized distributor to act as its local agent.
As part of our service to principals, we can assist in obtaining new product registration for principals that do not meet the criteria to register their own product in Indonesia. Our regulatory department stays up to date with Indonesian laws to ensure products are in compliance and launched on time.
UDC only distributes products that have been through the Indonesian government approval process and are from the original manufacturer.
