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Pharmaceutical Production Line
Finetech provides complete pharmaceutical production line solutions for capsules, tablets, powders and liquids.
Pharmaceutical Production Line Options
Our pharmaceutical production line includes raw material processing equipment (drying, mixing, granulation equipment); preparation equipment such as a tablet press and capsule filling machine; and packaging equipment (blister machine, cartoning machine). All machines can be combined inline system and comply with GMP standards to produce.
Granulation Line for Solid Dosage Forms
A granulation line is a series of machines designed to transform powders into granules, frequently used by the pharmaceutical industry. Since there are strict quality requirements for the content uniformity of the formed granules and their physicochemical properties, it is crucial to choose the right process. The wet granulation process ensures that the heterogeneous fine powder mixture is transformed into uniform granules with larger particle sizes and a greater density.
Blister Packaging Production Line
Our blister packaging line is designed for capsules and tablets. Our machines can complete the packaging of capsules, blister packs, vials and ampoules in one unit.
Pharmaceutical Bottle Packaging Line
Fully automatic bottle unscrambling, washing, filling, capping, foil sealing and labeling with minimal manual intervention.
Gummy Candy Production Line
A gummy candy production line is an integrated system designed for efficient, high-volume manufacturing of gelatin- or pectin-based candies.
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Customized production lines for your pharmaceutical factory
Application industries
FAQ
Here are some frequently asked questions about the pharmaceutical production line.
Typical stages include:
- Raw material dispensing
- Granulation (wet/dry)
- Mixing & Blending
- Compression (for tablets)
- Coating (if applicable)
- Encapsulation (for capsules)
- Inspection & Quality Control (QC)
- Packaging & Labeling
Key regulations include:
GMP (Good Manufacturing Practices) – FDA (US), EMA (EU), WHO.
ICH Guidelines (e.g., Q7 for APIs).
21 CFR Part 11 (Electronic Records Compliance).
ISO 13485 (Medical Devices, if applicable).
Our pharmaceutical production line equipment meets aseptic standards, but your production base needs to be equipped with an aseptic production workshop to ultimately achieve 100% aseptic production.
Yes, all of our pharmaceutical production equipment meets GMP standards.
Capsules, tablets, softgels, supplements, ointments, essential oils, oral liquids.