Manufacturing

Manufacturing / Packaging / Analysis

Meiji Seika Pharmatech Co., Ltd. produces a variety of antibacterial and generic drugs in solid dosage forms such as tablets and fine granules, as well as injectable drugs such as vials and pre-filled syringes. Leveraging the unique expertise and technological superiority developed by Meiji Seika Pharma, we will contribute to society by providing a stable supply of reliable products while enhancing our cost competitiveness.

Manufacture of solid preparations -> Manufacturing process for solid drugs

APIs and raw materials are weighed in a strictly temperature- and humidity-controlled room.
Granules are made using a granulator.
The tablets are formed into tablets in a properly adjusted tableting machine.
- > The mixed powder and/or granule are compressed into tablets in a properly adjusted tableting machine.
After inspecting the tablets for stains or cappings, they are printed on the tablets for easy identification.
Filling the PTP sheet with tablets securely.
The products will be placed in an outer box and packed properly.

Manufacture of pre-filled syringes -> Manufacturing process for prefilled syringes

The API and raw materials are prepared by well trained and educated workers and sent through a filter to an aseptic chamber -> aseptic area or room.
Fill the sterile syringe with the drug solution in a properly controlled aseptic chamber. -> aseptic area or room
We visually check the syringe after filling with great care that there are no scratches, leaks, or bubbles.
Securely attaching the plunger rod and finger grip to the syringe.
After accurately labeling the product, it is securely placed in a blister pack and sealed.
The products will be placed in an outer box and packed properly.

Quality Assuarance

We guarantee the quality of our products by ensuring they are manufactured according to methods approved by the pharmaceutical regulatory bodies and meet standards. We also conduct self-inspections of production activities in compliance with GMP, objectively review the status of manufacturing and quality control processes, and work to improve quality.