Esoma's quality approach is built around pharmaceutical discipline, documented processes and applicable Nigerian regulatory requirements.
The quality system should cover materials, processes, documentation, testing, storage and release — with responsibilities clearly defined.
Appropriate laboratory testing for incoming, in-process and finished materials.
Controlled records, traceability and appropriate batch documentation.
Defined processes and controls appropriate to each product.
Products should be released only through the company's approved quality process.
The site is intentionally prepared to display NAFDAC registration details, applicable certifications, manufacturing authorisations and other verified credentials. No certification or approval is claimed here without supporting company documentation.
Dedicated area for verified product registration and manufacturing information.
Dedicated area for verified Good Manufacturing Practice certifications or inspection information.
Space for approved labels, leaflets, specifications and product brochures.
