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US FDA Registered Facility

US FDA Registered Facility

Registration No. Verified

Our manufacturing processes align with US 21 CFR Part 111 current Good Manufacturing Practices (cGMP) for dietary supplements, allowing seamless export and product clearance in the United States.

WHO-GMP Certified

WHO-GMP Certified

World Health Organization Standards

Certified for consistent quality control, hygienic production layouts, cleanrooms, and comprehensive raw material testing to ensure zero contamination and complete batch-to-batch consistency.

FSSAI Compliant

FSSAI Compliant

Food Safety and Standards India

Authorized under central licensing for high-quality nutraceutical and dietary supplement manufacturing, meeting strict localized safety, packaging, and shelf-life compliance requirements.

Our Quality Management System (QMS)

We operate under a strict Quality Management System that bridges scientific research and commercial manufacturing. Every step of our contract manufacturing pipeline is documented, audited, and optimized to guarantee the performance and compliance of your supplement brand.

1

Raw Material Verification

Every incoming active, probiotic strain, and excipient is audited for identity, purity, heavy metal limits, and microbiological safety prior to formulation approval.

2

In-Process Quality Controls (IPQC)

We monitor temperature, relative humidity, water activity (Aw), and jelly brix values in real-time to preserve heat-sensitive probiotic strains during cooking and depositing.

3

Finished Product Validation

Every production batch undergoes analytical testing for label claims, including viability checks (CFU counts) and stability validation under accelerated conditions.

Export-Ready Dossier Compliance

Launching a supplement brand in international markets requires rigorous regulatory filings. Probiota Innovations provides complete technical dossiers for product registration across various jurisdictions, ensuring smooth customs clearances and retail onboarding.

North America & Europe

We support US FDA registration filings, Health Canada NPN applications, and European Union Food Supplement Directive compliance dossier preparations.

GCC, GCC-KSA, & TGA

Our facility provides the necessary documentation for TGA (Australia) compliance assessments and GCC (Gulf Cooperation Council) standard safety dossiers.

Partner with a Certified Manufacturer

We ensure your products meet global expectations in quality, performance, and scalability.

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