ISO 9001:2015 | WHO-GMP Certified

Quality Assurance & Compliance

Uncompromising compliance, standard testing protocols, and certified laboratories ensuring batch consistency

Uncompromising Excellence

Our Quality Commitment

At Eamon Drugs, quality is not a static milestone; it is the core foundation of our entire manufacturing philosophy.

Our quality assurance department ensures consistent product quality through checks at every stage, supported by a team of qualified and experienced professionals. The company delivers high-quality pharmaceuticals and nutraceuticals using advanced infrastructure, world-class technology, and skilled staff.

We maintain separate, independent Quality Control (QC) and Quality Assurance (QA) divisions. Our laboratories monitor every production stage, from raw active materials and packaging materials inspection to in-process parameters and finished batch clearance.

WHO-GMP & ISO 9001:2015
Eamon Drugs Quality Team and Facility
Complete Regulatory Dossiers
Instrumentation Dept.
Eamon Drugs Quality Control Laboratory
100% Raw Material Audits
QC Laboratory

Quality Control

Eamon Drugs has a dedicated Quality Control Lab, including a Microbiology Department, to conduct testing according to established specifications and standards. The lab is equipped with advanced analytical instruments operated by skilled, experienced analysts. All specifications and testing methods are approved by both the Quality Control and Quality Assurance Departments.

Sophisticated Analytical Instruments:

HPLC Systems
UV-Vis Spectrophotometer
Dissolution & DT Tester
Karl Fischer Titrator
Polarimeter & Refractometer
Sterile Laminar Hoods
Quality Assurance

Quality Assurance

The Quality Assurance Department ensures consistent product quality through audits and checks at every production stage.

Supported by a highly qualified and experienced team, Eamon Drugs maintains a high standard of quality for both pharmaceutical and nutraceutical products, utilizing top-tier infrastructure, cutting-edge technology, and expert staff.

From raw materials sourcing to standard packaging line audits, our QA protocols ensure complete traceabilities, document logs, compliance audits, and clean validations matching global CDMO expectations.

QA Operations
Eamon Drugs Quality Assurance Procedures
100% Batch Traceability
Laboratory Divisions

Testing & Compliance Units

Comprehensive analytical testing facilities housed within our plant

Chemical Analysis Instrumentation Laboratory

Chemical Analysis

Precise active substance identification and assay tests using state-of-the-art analytical instrumentation.

  • HPLC chromatography checks
  • UV-Vis Spectrophotometry
  • Karl Fischer moisture check
Review Specifications
In-Process Quality Control Capsule Testing

In-Process Controls

Real-time physical testing conducted directly on encapsulation and topical filling lines.

  • Softgel shell thickness monitoring
  • Fill weight variation controls
  • Seal audits and leakage assays
Review Specifications
Microbiology Laboratory Sterile Environmental Testing

Microbiology Laboratory

Strict microbial screenings conducted in sterile, positive-pressure environment chambers.

  • Total bacterial & fungal counts
  • Pathogen checking (E. coli, Salmonella)
  • Purified water system loops monitoring
Review Specifications

Request Auditing & Tech Dossiers

We provide transparent access to our standard quality logs, compliance files, and licensing details for prospective clients.

Request Dossier Access