Compliance - Celmark International
We are dedicated to quality control in supplement manufacturing, conducting FDA inspections, staying cGMP-compliant and keeping a certified-organic status.
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From conducting frequent FDA inspections and chemical testing, to having an up-to-date cGMP-compliant and organic-certified status, we’re committed to quality control.

Quality comes first.

At Celmark International Inc., we proudly operate in an FDA-inspected, cGMP-compliant and organic-certified facility, and are dedicated to providing top-notch quality control at all stages of the manufacturing process. Some of the ways we achieve this include:

  • Incoming chemical-analytical testing
  • Incoming chemical-bacteriological testing
  • Batch-bacteriological testing
  • After-fill bacteriological testing
  • Production-line sampling
  • Ongoing audits performed by key clients supplement categories.
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Our team also performs other extensive HPLC testing, which includes structured methods and validation, wet chemistry testing, microbiological testing and stability testing. Standard operating procedures cover all aspects of production, including facilities, equipment, components and closures, production processes, sanitation and maintenance, packaging and labeling, with requisite record keeping and controls at every stage.

Additionally, we have an on-site, full-service analytical and microbiological laboratory that’s staffed with a microbiologist and stocked with state-of-the-art equipment. We also provide ongoing internal training programs for our staff that are taught by our in-house experts of each appropriate discipline, allowing our team to function quickly and effectively at all times.