Integrity By Design: The CAPTEK Pharma Softgel Center Of Excellence

A US FDA 21 CFR Part 210/211-compliant facility capable of producing more than 3 billion capsules a year, CAPTEK Pharma’s 54,000 sq ft manufacturing facility in La Mirada, California is a Softgel Center of Excellence.

The facility has been purpose-built for the development and manufacture of pharmaceutical softgels, designed from the ground up to provide your project with the utmost in product integrity.

From the very earliest planning stages it was built with a single purpose: to maximize the efficiency and integrity of bulk softgel manufacturing for our customers. Every detail of the facility has been painstakingly developed with that goal in mind.

The Latest In Advanced Technologies And Instrumentation

The facility’s design is based on a U-shaped process flow diagram. This design enables a streamlined end-to-end process flow that utilizes process personnel and material flow to their fullest advantage. Line redundancies have been built into the facility’s design from the start to ensure that nothing jeopardizes the consistent supply of your product.

The La Mirada facility is equipped with cutting-edge technology and equipment, and its on-site laboratories feature the latest in advanced technologies and instrumentation.

Legacy Of Softgel Manufacturing Quality

CAPTEK’s 20+ year history has given us an in-depth knowledge of cGMP manufacturing and formulation equipment, and we’ve outfitted our pharma facility with top-of-the-line components for producing softgels of the highest quality.

All of our equipment and technologies have passed rigorous engineering installation, operation, and performance qualifications.

Of course, the most important components of the La Mirada facility are CAPTEK Pharma’s knowledgeable, well-trained employees. Our talented and experienced team has knowledge of softgel manufacturing unmatched in the industry.

Speak With An Expert

Profile Photo: Hiren Patel

Hiren Patel

Quality & Validation Specialist

Hiren offers 28 years of pharmaceutical development and manufacturing experience with emphasis on product/process development, validation and quality. Hiren also leads the quality unit and CAPTEK’s product development/validation team. With his oversight of product development, validation and quality at Captek Pharma, Hiren is prepared to discuss any challenges on your upcoming project.

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