Our Accreditations | Allrite Group

Global Compliance & Quality Assurance

At Allrite Group, regulatory compliance is the cornerstone of our manufacturing philosophy. Operating with absolute adherence to strict Quality by Design (QbD) principles, we view compliance not as a checklist, but as a commitment to de-risking the global supply chain.

Our facilities operate in a state of perpetual "audit-readiness," holding active validations from leading national and international regulatory authorities to seamlessly support our partners across the East African and ASEAN trade corridors.

Global Quality Standards & National Foundations

WHO-GMP (World Health Organization - Good Manufacturing Practice)

This globally recognized certification ensures that all six of our dedicated manufacturing blocks consistently produce therapeutics to the highest safety, efficacy, and quality standards, minimizing risk across every batch.

CDSCO (Central Drugs Standard Control Organization - India)

Our foundational manufacturing license granted by India’s national regulatory body, validating our operational integrity, facility design, and capacity to manufacture massive-scale OSD, liquids, and external preparations.

GLP (Good Laboratory Practice)

Our R&D and Quality Control laboratories operate under stringent GLP protocols. This certification guarantees absolute data integrity, reproducibility, and reliability for all analytical testing and international regulatory submissions.

AYUSH Accreditation

A specialized national certification for our dedicated traditional and herbal medicine manufacturing block, applying rigorous modern quality controls to alternative therapeutics to ensure zero cross-contamination with our synthetic pharmaceutical lines.

International Market Validations (Export Corridors)

To facilitate rapid market access for our global B2B partners

Cambodia GMP (Ministry of Health, Kingdom of Cambodia)

Our latest international milestone (License No. CAM N0021PM-26) officially certifies our Unit-I facility. This GMP validation serves as our primary regulatory anchor for the high-volume export of General Tablets, Capsules, and External preparations into the rapidly growing ASEAN market.

TMDA (Tanzania Medicines and Medical Devices Authority)

An active, highly respected validation that acts as our gateway for the East African corridor. Our TMDA status provides international partners—including those operating in neighboring regions like Uganda—with the assurance of a gold-standard regulatory benchmark.

Partner with an Audit-Ready CDMO

Our Regulatory Affairs and Quality Assurance teams are equipped to provide comprehensive Site Master Files (SMF) and virtual QA walkthroughs to prospective partners.

Request CTD Dossier List or SMF