Our Services

At Caribbean Scientific, we specialize in calibration, preventive maintenance, validation, and repairs that ensure top-notch quality assurance and minimal downtime. We serve laboratories, hospitals, pharma, and everything in between. Our Services in Puerto Rico include:
  • Calibration: Accurate measurements are vital. We calibrate a wide range of equipment, including particle counters, cold storage, ambient control, heat control, light meters, centrifuges, microscopes, and more.
  • Preventive Maintenance: Stay ahead of potential issues. Our experts provide thorough maintenance to keep your equipment running smoothly, minimizing disruptions to your operations.
  • Repairs: When equipment falters, we're here to restore it. Our skilled technicians diagnose and repair your instruments efficiently to get you back on track.
Why Choose Us: 🔬 Industry Expertise: With over 30 years of experience, we understand the unique demands of the Puerto Rico market. Discover how Caribbean Scientific can optimize your equipment's performance and bolster your quality assurance. Contact us today to elevate your operations! #CalibrationServices #PreventiveMaintenance #EquipmentRepairs #QualityControl #PuertoRicoServices #IndustrialEquipment #OptimizedPerformance"
 

Calibration

We offer the calibration of your equipment to minimize any measurement uncertainty by ensuring the accuracy of test equipment, in other words to ensure the readings are consistent with certified measurements. Calibration quantifies and controls errors or uncertainties within measurement processes to an acceptable level.

Certification

When we certify your equipment we ensure that it is operating as per manufacturer spec and within calibration of the measurement uncertainties. This is a service that ensures your equipment is currently operating at it’s optimal performance.

Preventive Maintenance

Our goal is to partner with our customers to develop a successful preventive maintenance program, to establish consistent practices that we have designed to improve the performance and safety of the equipment. This developed maintenance program will help to improve equipment life and avoid any unplanned maintenance activity.

Benefits of keeping a preventive maintenance program:

  • Equipment downtime is decreased and the number of major repairs are reduced, conserving the asset to a longer life.
  • Better conservation of assets and increased life expectancy of assets, an improvement on equipment reliability.
  • Reduced overtime costs and more economical use of maintenance workers due to working on a scheduled basis instead of a crash basis to repair breakdowns
  • Timely, routine repairs circumvent fewer large-scale repairs, overall COST SAVINGS

Provide us with a list of your equipment to develop a time based Preventive Maintenance program.

Repair

We have developed a service team to ensure all repairs are performed by manufacturer trained technicians. The team has specialized in the following equipment:

  • Ultra Low Refrigeration repairs
  • Critical cold storage equipment repairs (Lab Refrigerators/Freezers, Vaccine storage units)
  • Lab Incubators and Heat controlled equipment
  • Particle Counters (viable/non-viable)

Inquiry below with your needs and we will help in any way we can.

Validation Services

We also provide validation services and have an extensive file of qualification protocols for laboratory equipment, so our customers can install and operate their new equipment without delay. We are able to provide our customers with customized sales and service solutions to suit their individualized needs.

Installation Qualification (IQ)

Installation qualification, or IQ, is a documented verification process that the instrument or piece of equipment has been properly delivered, installed, and configured according to standards set by the manufacturer or by an approved installation checklist.

Installation qualification requirements for equipment include checking for proper location, proper energy supply, and acceptable environmental conditions.

Operational Qualification (OQ)

Operational Qualification is the next step in quality assurance and involves testing the equipment and ensuring it performs as specified, within operating ranges as listed by the manufacturer. All aspects of the equipment receive individual testing, and the tester documents the proper operation of each.

Operational Qualification for equipment is necessary after installation, significant maintenance, or modifications to the equipment, or as a feature of scheduled quality assurance testing.

Performance Qualification (PQ)

Before your equipment can be truly rated as qualified, you will need to put it through performance qualification. Your process performance qualification protocol will feature verification and documentation that all equipment is working within the accepted range as specified, does it perform as expected under real conditions. All instruments are tested together according to a detailed test plan and must generate reproducible results.

Method Transfer Validation

Method transfer is the documented process that qualifies a laboratory to use a test procedure that originated in another laboratory. The validation of a method is the process that confirms the suitability of the method for its intended analytical use.

Testimonials

“With over 30 years of experience, FIS VCI Inc is a distributor of laboratory and process equipment, instrumentation, and supplies, for the pharmaceutical and biotechnological manufacturing industry and the educational laboratory. A family owned business; it was founded in 1984 by Do単a Eva Azizi under the name of Filtration Instrumentation Specialist, Inc. (FIS) with a single sales division. In 1993 a sister company was founded to provide service to the equipments sold by FIS under the name of VCI, Inc. In 2000 the companies merged to form what is
known today as FIS VCI.”

Marketing Executive, Ryan

“With over 30 years of experience, FIS VCI Inc is a distributor of laboratory and process equipment, instrumentation, and supplies, for the pharmaceutical and biotechnological manufacturing industry and the educational laboratory. A family owned business; it was founded in 1984 by Do単a Eva Azizi under the name of Filtration Instrumentation Specialist, Inc. (FIS) with a single sales division. In 1993 a sister company was founded to provide service to the equipments sold by FIS under the name of VCI, Inc. In 2000 the companies merged to form what is
known today as FIS VCI.”

Software Developer, John Doe

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