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Quality Policy

Our commitment to international quality control, GMP guidelines, and validation protocols.

Our Quality Policy

Quality is the cornerstone of all operations at AQUA OVERSEAS LLP. As a global exporter of life-saving medicines, we maintain a stringent Quality Assurance (QA) protocol that covers the entire lifecycle of sourcing, checking, storing, and exporting.

We work exclusively with certified manufacturing facilities. Each facility is audited to ensure compliance with strict environmental parameters, sterile zones, and active validation controls.

Quality Control Lab

Key Guidelines of Our Quality Standards

GMP Audited Plants

We exclusively select suppliers whose facilities strictly adhere to WHO-GMP norms, cleanroom classification standards, and ISO 9001 certifications.

Batch Integrity

Every batch exported is accompanied by a Certificate of Analysis (CoA), Free Sale Certificate (FSC), and Batch Manufacturing Record (BMR) data where applicable.

In-Transit Safety

Pharmaceuticals and sensitive diagnostic materials are packed in customized temperature-controlled insulated cartons to ensure formulation integrity during shipment.

Strict Sourcing Limits

All Product are in compliance with pharmacopeial Guidance and inhouse specification.

Our Quality Assurance Journey

1

Plant Sourcing

Auditing manufacturing plants for WHO-GMP compliance.

2

Analysis Verify

Inspecting batch Certificates of Analysis (CoA).

3

Custom Packing

Custom pack layout and thermal boxing coordination.

4

Secure Export

Direct shipping and consular legalization tracking.

Our Certification Sourcing Target

Our goal is to ensure 100% compliance with client country import guidelines. We assist with documentation verification, stability data studies (Zone IVb compliance), and certificate validation with local consulates.

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