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Coastal Life Technologies' new 40,000 square foot headquarters opens.

Coastal Life Technologies (CLT), an outsource manufacturer and distributor of sterile, single use medical devices has opened its new headquarters in San Antonio, Texas. The newly-constructed 40,000 square foot space has been developed to maximize efficiencies and accommodate the growth of the company. The facility includes:

 

  • ISO Class 8 Clean Room with 8,000 square feet
  • Over 20,000 square feet of climate-controlled warehouse space
  • State-of-the-art technology and equipment
  • Computerized tracking system for distribution
  • Central location for efficient order fulfillment.

 

CLT President Paul Muller and General Manager David Huff were integral in the design of the facility, which broke ground almost a year ago. "We have increased our space exponentially to accommodate the needs of our clients and the growth of our company. In developing this facility, we looked at the latest technologies and building methods to ensure quality control and efficiency, and we are delighted to be at home here," said Muller. CLT provides streamlined solutions for manufacturers of medical devices, including design and engineering, raw material management, final assembly and sterile packaging, management of the sterilization process and warehousing and distribution of product. The company's clients include companies from around the world.

Final Assembly & Sterile Packaging

CLT can perform a variety of assembly processes and packaging operations in our 8,000 square foot ISO Class 8 clean room. Our primary expertise is in assembling and packaging sterile, single-use, disposable surgical devices.

We engineer processes and streamline manufacturing to allow for greater efficiencies, lowering cost to our customers. Our team reviews the specific assembly requirements and selects the best systems for the product. Lean Manufacturing tenets such as pull systems, back flushing, and Kanbans are utilized to maintain and maximize production control and efficiency.

Product quality should not depend on inspection after production; it should be inherent to the design and manufacturing processes. Quality is always a part of our process engineering. A quality assurance plan suited to your product requirements will be established, including the quality benchmarks used in our continuous improvement efforts.

Process validation is integral to the final packaging of all sterile devices that we manufacture. We can package in pouches or trays depending on what is best suited for your product. CLT continues to monitor the packaging process as part of our ongoing quality plans to ensure package integrity.