Vantage Point Global Labs

The laboratory

Licensed THC and natural products manufacturing laboratory in El Guarco, Costa Rica

The facility in El Tejar, El Guarco receives EU-GACP certified flower and manufactures cannabis based medicines under licence from the Ministry of Health.

Lush mountain landscape of the Costa Rican Central Valley near El Guarco, Cartago.

Facility

Built for manufacturing, not for display

The laboratory sits in El Tejar, El Guarco, in the province of Cartago, at the eastern end of Costa Rica's Central Valley. It was designed around one flow: flower in, tested medicine out.

Separate areas handle receipt and quarantine, extraction, formulation, filling, packaging and quality control. Materials move forward through the building, never backwards.

Technician in full cleanroom gowning weighing finished product on an analytical balance in the El Guarco laboratory.
Location
El Tejar, El Guarco, Cartago, Costa Rica
Licence
Resolution MS-DRPIRS-1894-2026
Effective
19 August 2026
Scope
Manufacture of cannabis based medicines
Supply
EU-GACP certified flower from Hybrida Farms

Licence

What the licence covers

The Ministry of Health authorised the manufacture of cannabis based medicines at this facility by Resolution MS-DRPIRS-1894-2026, effective 19 August 2026. We describe our authorisation in exactly those terms and nothing wider.

  • Licensed by the Ministry of Health to manufacture cannabis based medicines.
  • Manufacturing is limited to the licensed facility in El Guarco, Cartago.
  • Incoming flower comes from EU-GACP certified cultivation at Hybrida Farms.
  • We are licensed. We do not claim GMP or pharmaceutical certification.

Process

Five stages, each documented

MANUFACTURING: GMP / THC products formulated and produced

  1. 01

    Receipt

    Dried flower arrives from Hybrida Farms with batch documentation, is weighed, reconciled and held in quarantine until sampling is complete.

  2. 02

    Extraction

    Approved material is extracted under controlled, recorded parameters. Yields and solvent records are reconciled per batch.

  3. 03

    Formulation

    Extracts are standardised and formulated into the target presentation: oils, syrups or tablets, against a written specification.

  4. 04

    Filling and packaging

    Product is filled, closed, labelled and coded in a controlled area, with line clearance and reconciliation records.

  5. 05

    Testing and release

    Each batch is tested for potency, purity, microbiology, heavy metals, pesticides and mycotoxins. Documentation is reviewed before release.

Stainless steel closed loop extraction vessel being operated by a gowned technician in the manufacturing suite.
Gowning corridor and airlock leading into the classified manufacturing rooms.

Team

The people responsible

The laboratory is run by a Costa Rican management team working alongside our cultivation colleagues at Hybrida Farms.

Name to be confirmed

Laboratory Director

Oversees daily laboratory operations, batch records and regulatory liaison with the Ministry of Health.

Name to be confirmed

Head of Manufacturing

Manages extraction, formulation, filling and packaging operations in the controlled manufacturing suite.

Name to be confirmed

Head of Quality and Compliance

Owns quality assurance, batch release, documentation control and compliance with national and international standards.

Name to be confirmed

Head of Analytical Services

Manages potency, purity, microbiology and contaminant testing plus method validation and instrument qualification.

Arrange a technical conversation

Licensed importers, distributors and research partners can request the compliance pack and speak with the team in Cartago.

Enquiry