TURNKEY PHARMACEUTICAL PREPARATION & PACKAGING
Drug Preparation / Packaging Facilities
Integrated formulation, dosage-form processing, filling, blistering, bottling, serialization, cartoning and quality-control infrastructure—from project definition to operational transfer.
Request a feasibility study ↗INFINITY PHARMACEUTICAL PLATFORMPrepare · process · fill · inspect · serialize · package
Portfolio-ledProcess defined by dosage form
GMP-orientedControlled people and material flow
TraceableBatch and unit-level identification
TurnkeyPlant, process and training
Build an operating pharmaceutical platform—not disconnected machines.
Infinity structures the facility around the approved portfolio, annual demand, batch sizes, dosage forms, packaging formats, localization level, quality pathway, utilities and workforce model.
One controlled facility.
Multiple market formats.
01
Tablets and coated tablets
02
Hard-gelatin capsules
03
Oral liquid preparations
04
Topical creams and gels
05
Sterile liquid vials where included
06
Powder and granule sachets
07
Bottle and blister presentations
08
Secondary packaging and serialization
Final products, formulations and claims depend on approved technology transfer, development, validation and regulatory authorization.
Controlled from incoming material to serialized batch release.
Sampling and incoming QC
Dispensing and weighing
Preparation or granulation
Dosage-form processing
In-process quality controls
Primary filling or packaging
Inspection and serialization
Secondary packaging
Batch review and release
FACILITY & CONTAMINATION CONTROL
Designed around product, people and material flow.
Materials, personnel, packaging components, product, waste and cleaning routes are mapped to protect quality, reduce mix-up risk and support efficient changeover.
01Raw-material quarantine
02Sampling and dispensing
03Formulation and preparation
04Granulation and drying
05Tablet / capsule processing
06Controlled liquid filling
07Primary packaging
08Secondary packaging
09QC chemistry laboratory
10Microbiology laboratory
11Wash and equipment storage
12Finished-goods quarantine
The complete preparation and packaging ecosystem.
Systems are selected against dosage form, batch size, containment need, packaging material, line speed, serialization level and local serviceability.
Dispensing and weighing booths
Jacketed formulation vessels
High-shear mixers and granulators
Tablet presses and coaters
Capsule filling machines
Liquid and vial filling systems
Blister and strip packaging lines
Bottle counting and capping
Labeling and serialization cameras
Cartoners and case packers
Metal detection and checkweighing
QC and microbiology laboratories
CAPACITY & FORMAT STRATEGY
Right-sized for the portfolio. Designed to expand.
The model connects batch size, process yield, changeover, packaging speed, shifts, QC sampling, warehouse demand and expected SKU mix.
- Single- or multi-dosage-form facilities
- Blister, bottle, sachet and vial formats
- Manual to automated packaging pathways
- Expandable preparation and packaging modules
- Future product and warehouse zones
From portfolio decision to released pilot batches.
Feasibility
Portfolio, volume, site and market model
Product strategy
Dosage forms, pack formats and localization
Concept design
Process, zoning, flows and utilities
Equipment URS
Capacity, automation and interfaces
Detailed engineering
Clean areas, HVAC, MEP and layouts
Procurement
Process, packaging, laboratory and utilities
Installation
Placement, connection and commissioning
Qualification
DQ/IQ/OQ and process-readiness support
Technology transfer
Documents, methods and personnel training
Pilot batches
Optimization, packaging trials and ramp-up
QUALITY & REGULATORY READINESS
Evidence and traceability built into every batch.
The program can cover material qualification, in-process controls, cleaning strategy, process and packaging validation, analytical method transfer, stability, data integrity and batch documentation.
GMP-oriented designMaterial traceabilityCleaning validationProcess validationPackaging validationSerializationData integrityStability planning
A pharmaceutical production and packaging operating system.
✓ Portfolio and capacity feasibility
✓ Facility concept and detailed layouts
✓ Process and packaging equipment URS
✓ Clean utilities and HVAC requirements
✓ QC and microbiology laboratories
✓ Procurement and installation coordination
✓ Qualification and validation framework
✓ Technology and analytical-method transfer
✓ SOP, batch and packaging documentation
✓ Training, pilot batches and ramp-up
Transform pharmaceutical demand into regional manufacturing capability.
Share your country, target dosage forms, annual volumes, package formats and site status.
Start the pharmaceutical facility discussion ↗