We ensure your company with the combination of legal, administrative, and technical measures that government ensure to take safety.

We help your company with Current Good Manufacturing Practises (cGMP – ICHQ7) .

We help with Good documentation practice in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.

We help companies with quality management system (QMS), a system that documents the policies, business processes, and procedures necessary for an organization to create and deliver its products or services to its customers, and therefore increase customer satisfaction through high product quality.

We help with laboratory QMS, which is a systematic, integrated set of activities to establish and control the work processes from preanalytical through postanalytical processes, manage resources, conduct evaluations, and make continual improvements to ensure consistent quality results.

We help with any professional service or creative work requiring engineering education, training and experience and the application of special knowledge of the mathematical, physical and engineering sciences.

We help you know the utmost importance of Quality Culture in a Pharmaceutical Company. Quality Culture should be linked with Data Integrity, and we’ll ensure your company achieves it.

We help your company to achieve the ability of an organization to operate at a level that allows for effective preparation for an inspection.

We help with Electronic Common Technical Documents (eCTD) reviews and readiness.