Oral solid dosage
Tablets and capsules manufactured under controlled, documented conditions.
Manufacturing
Controlled processes. Consistent products.
From incoming materials to dispatch, our manufacturing operations are organised around documented procedures, trained people and quality checks at every stage.
Production capabilities
Dosage forms we manufacture
Capabilities marked “To confirm” must be verified before publishing.
Oral liquids
Syrups, solutions and suspensions with controlled mixing and filling.
- To confirm
Sterile preparations
[CONFIRM] Injectable manufacturing capability — verify before publishing.
- To confirm
Topicals & softgels
[CONFIRM] Creams, ointments, gels and soft gelatin capsules — verify before publishing.
Manufacturing process
From material receipt to dispatch
Each stage is governed by standard operating procedures and recorded in the batch manufacturing record.
Step 01
Material receipt & sampling
Incoming raw and packaging materials are quarantined, sampled and tested before approval.
Step 02
Dispensing
Approved materials are weighed and dispensed in controlled areas against the batch record.
Step 03
Formulation & processing
Granulation, blending, compression, filling or compounding follow validated batch instructions.
Step 04
In-process controls
Critical parameters are checked during production so deviations are caught early.
Step 05
Packaging & labelling
Primary and secondary packaging with line clearance and label reconciliation.
Step 06
QC testing & QA release
Finished products are tested and batch documentation reviewed before release.
Step 07
Storage & dispatch
Released goods are stored under specified conditions and dispatched with full traceability.
Manufacturing facilities
Facilities designed for orderly, controlled production
Production areas are organised to support logical material and personnel flow, cleanliness and environmental control appropriate to each dosage form.
- Segregated production areas by dosage form
- Controlled environmental conditions
- Documented cleaning and line clearance
- Calibrated and maintained equipment
- [FACILITY LOCATION & AREA]
- [KEY EQUIPMENT — only if verified]
Packaging & warehousing
Protecting product integrity through to delivery
Packaging and storage are treated as part of product quality — with checks for correct materials, coding and storage conditions.
- Blister, strip, bottle and carton packaging formats
- Batch coding, expiry printing and label reconciliation
- Segregated storage for quarantined, approved and rejected goods
- FIFO / FEFO stock management
- [STORAGE CONDITIONS — e.g. temperature-controlled areas, if applicable]
Operational standards
Quality, safety and compliance at every step
Manufacturing facilities
Production areas designed for orderly material and personnel flow, with environmental controls appropriate to each dosage form. [FACILITY DETAILS]
Quality control
Sampling and testing of raw materials, in-process samples and finished products by trained analysts.
Packaging
Blister, strip, bottle and carton packaging with line clearance, coding and reconciliation checks.
Warehousing
Segregated storage for quarantined, approved and rejected materials with FIFO / FEFO practices.
Safety
Occupational health and safety practices, personal protective equipment and regular training.
Regulatory standards
Operations aligned with applicable Good Manufacturing Practice requirements. [SPECIFY STANDARDS]
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