We develop integral projects for global markets.
We have many years of experience in architectural projects and constructions of laboratories and clean rooms of different nature and complexity, we incorporate specific facilities for a variety of industries:
Definition of main and secondary objectives. Matrix idea. Study diagrams. Sustainability guidelines.
Implementation analysis. GMP Standards Approach. Conditioning Approach. Conditioning approach.
Basis Project ( plants, cuts, facades, 3D ). Efficiency & Energy Saving Criteria. Preliminary constructions systems, materials and technology.
Development of the technical project ( masonry, structure, facilities). Furniture design, equipment layout. Technical memories. Landscaping . User´s manual for the Facility.
Preparation & Assembly of sheets. Call for contractor companies. Bid evaluation. Technical judgment for business allocation.
Construction Comptroller. Technical Management. Supervision & Monitoring.
Good Manufacturing Practices is a system for ensuring that pharmaceutical products are consistently produced and controlled, according to quality standards. It covers all aspects of production, from starting materials, premises and equipment to training and personal hygiene of staff.
Good Distribution Practices describes the minimum standards that a wholesale distributor must meet to ensure that the quality and integrity of pharmaceutical products is maintained throughout the supply chain. Also applies for sourcing, storage and transportations of active pharmaceutical ingredients as well as other elements used in the production.
Good Laboratory Practices is a quality system of management controls for research laboratories and organizations, to try to ensure the uniformity, consistency, reliability, reproducibility, quality and integrity of analytic results.
