Pharmaceutical Export Coordination — Eswatini
MHRA-Governed Pharmaceutical Exports With GDP-Verified Traceability
Eswatini’s pharmaceutical procurement structure is defined by regulated public-sector import pathways, private importers, and programme-supported initiatives requiring clear documentation and validated processes. GPD exports exclusively from an MHRA-licensed UK facility, meeting full Good Distribution Practice (GDP) expectations across preparation, packing, and dispatch. Our export documentation aligns with the requirements expected by institutions under the governance of bodies such as the Eswatini Medicines Regulatory Authority (EMRA).
GDP-Consistent Export Records Supporting Regulated Import Requirements
GPD provides documentation packages aligned with institutional procurement needs, including: Verified batch and traceability documentation. Packaging integrity records. Verified temperature logs across the logistics chain. These support transparent, audit-ready review processes.
Maintaining Stability Across Warm-Climate Transit Conditions
Eswatini’s warm climate requires disciplined temperature-control management. GPD employs validated cold-chain systems and calibrated monitoring devices to maintain and document temperature integrity.
Validated Cold-Chain Systems
Validated cold-chain systems maintain stable temperatures across warm-climate transit conditions.
Calibrated Monitoring Devices
Calibrated monitoring devices continuously record temperature integrity throughout distribution processes.
Compliance-Ready Temperature Records
Documented temperature data supports compliance with institutional and regulatory requirements.
Aligned Export Coordination for Public and Private Import Frameworks
Eswatini’s procurement environment includes regulated private-sector importers, public institutions, and health programme partners. GPD aligns with these channels through consistent documentation, GDP-governed handling, and structured communication through our compliance unit.
Controlled Access to Export Documentation Under MHRA Standards
Authorised importers or procurement organisations may request documentation through GPD’s compliance office.