Capabilities & Qualifications


All Tower Labs manufacturing facilities are registered with the U.S. FDA and are cGMP compliant.


FDA Registered & cGMP Compliant Manufacturing Facilities

All of Tower Laboratories’ facilities are registered with the FDA and are cGMP compliant. Tower Laboratories has a robust quality system that consistently meets the audit requirements of customers and applicable agencies. Tower Laboratories regularly conducts employee training. Good documentation practices, product validations, and procedures for corrective & preventive action are examples of quality system components that are in place and embraced.


In-House Testing

Tower Laboratories has extensive testing capabilities. All materials are tested and approved in our Quality Control laboratories prior to use, and finished products are tested to confirm they meet specifications prior to release. Our laboratories also support our Product Development Scientists as pertains to all analytical testing including formal and accelerated stability testing. Lab equipment and capabilities include HPLC, AA, IR, UV/Vis spectroscopy, and standard wet and dry analytical instrumentation.


OTC Drugs, Medical Devices, Supplements

Tower Laboratories manufacturers products that cover a wide array of regulatory classifications including OTC and prescription drugs, medical devices, supplements, cosmetics, and non-regulated.  Our Compliance Department can assist with applicable regulatory filings, product labeling requirements, etc.


Humidity Controlled Environment

A low humidity environment is critical for the production of stable effervescent products. As a result of our 35+ years experience, Tower Laboratories has developed proprietary knowledge pertaining to the environments and processes that are critical to our business. This expertise differentiates us significantly from our competition and makes us the ‘go to’ source for companies who are looking for a best-in-class partner to develop and produce their effervescent products.