Business Details
Trusted Vitamin Supplement Manufacturing Services
Bayshore Pharmaceuticals has established itself as a leader in contract manufacturing for vitamin and dietary supplements. With a management team boasting 40 years of combined experience in generic pharmaceuticals, private label production, and contract manufacturing, we provide comprehensive solutions from concept to launch. Our expertise in oral liquid dosage forms is supported by a robust network of research organizations, contract manufacturers, and industry relationships that span 90% of key players in the U.S. pharmaceutical and nutraceutical markets. Our Tampa, Florida facility operates under cGMP certification with on-site quality control, third-party analytical testing, and adherence to FDA 21 CFR 111 guidelines. We specialize in turn-key services including formulation development, stability testing, regulatory compliance, and packaging for products ranging from 30 mL to 16 oz containers.Our commitment to quality is demonstrated through rigorous vendor qualification, ISO 17025 testing capabilities, and a 5 million unit annual production capacity. By maintaining agility without compromising integrity, we help clients navigate the complexities of healthcare product development and distribution. Our facility's full-release testing for micro and assay parameters ensures product safety and purity meet the highest industry standards. Through strategic partnerships and internal expertise in sales, marketing, and business development, we deliver tailored solutions that address evolving market demands. Our track record of successful collaborations with major industry players positions us as a trusted partner for healthcare innovation.
Services
Product Development
Formulation Testing
Stability Studies
Regulatory Compliance
Liquid Filling
Packaging Services
Quality Control
Distribution Support
Highlights and features
- 40+ years combined management experience in pharmaceutical contract manufacturing
- Established relationships with 90% of U.S. pharmaceutical industry key players
- Turn-key services from product development to distribution
- cGMP-certified facility with on-site quality control
- ISO 17025 testing capabilities for product verification
Associations and certifications
- FDA
- cGMP
- ISO 17025
Services
Product Development
Our team develops customized liquid supplement formulations tailored to client specifications. We conduct stability studies, perform compatibility testing, and optimize delivery methods while maintaining compliance with FDA regulations. With expertise in oral dosage forms, we ensure product efficacy and shelf stability through rigorous development protocols.
Quality Control Testing
We implement comprehensive quality control measures including microbial testing, chemical assays, and purity verification. Our facility maintains cGMP certification with on-site testing capabilities and access to ISO 17025-verified third-party laboratories for independent product validation and regulatory compliance assurance.
Contract Manufacturing
Our Tampa facility offers scalable manufacturing solutions for liquid supplements with batch capacities from 2,500 to 25,000 units. We handle complete production cycles including mixing, filling, packaging, and quality assurance for private label and branded products under strict regulatory compliance.
Regulatory Compliance
We provide expert guidance through FDA 21 CFR 111 compliance requirements for dietary supplements. Our services include label review, documentation preparation, and quality system implementation to ensure adherence to current good manufacturing practices and market approval requirements.
Packaging Solutions
Our facility offers comprehensive packaging services for liquid supplements including primary and secondary configurations. We handle labeling, bottle selection, and closure systems while ensuring compliance with safety standards and market-specific requirements for both domestic and international distribution.
People
Management Team
Executive Leadership
Bayshore's leadership team brings 40+ years of combined experience in pharmaceutical contract manufacturing, private label production, and industry sales. Their expertise spans regulatory compliance, product development, and strategic partnerships with major healthcare market players.
Questions
What services does Bayshore Pharmaceuticals offer?
We provide full-service contract manufacturing for liquid vitamins and supplements, including formulation development, testing, regulatory compliance, filling, packaging, and distribution support.
Are your manufacturing facilities FDA-registered?
Yes, we operate an FDA-established facility in Tampa, FL with on-site quality control and compliance to 21 CFR 111 guidelines for dietary supplements.
What quality assurance measures do you implement?
Our cGMP-certified facility conducts full-release testing, maintains rigorous vendor qualification standards, and offers ISO 17025 product verification upon request.
What production capacities do you have available?
We handle batch sizes from 2,500 to 25,000 units with fill sizes ranging from 30 mL to 16 oz containers and annual production capacity up to 5 million units.
How do you ensure product safety and purity?
All products undergo third-party analytical testing, microbial analysis, and chemical assay verification to guarantee safety, purity, and potency.
Can you help with regulatory compliance for supplements?
Our team provides comprehensive regulatory support including label review, documentation preparation, and compliance strategy for FDA and state requirements.
