Quality Assurance

The quality assurance system of Transparent Labs USA covers all activities and aspects of production and management cycles, as well as other activities related to their possible influence on the quality of the production and services.

All functions and responsibilities related to quality assurance are in accordance with the requirements of GMP (good manufacturing practice) and are specified in the relevant job descriptions, instructions, procedures and other proprietary documents.

The quality assurance system covers all technological processes (from supply to distribution and aftersale) as well as non-technological processes, for the purpose of their coordination and directing them to achieve the final goals of the company – maintenance and development of overall high quality of production and full customer satisfaction.

Important aspects of the company’s quality assurance system are:
- assessments and maintenance of suppliers, whose production and services correspond to the company’s policy for compliance with the requirements of the management systems declared by them.
- ongoing audits;
- the process of release of the final product;
- inspections carried out and self-inspections conducted on all elements of GMP;
- systematic use of the reports of self-inspections and inspections as a basis for development and improvement of the company’s policy.

The Company's quality control is carried out in analytical, chromatographic and microbiological laboratory, where narrowly-specialized and highly-qualified specialists work. It is noteworthy that Transparent Labs USA is among the few drug manufacturing companies that have their own microbiological laboratory which guarantees the microbiological purity of products

Quality control is applied to all of the following, without exception: received active substances; other raw materials, supplementary materials, materials and packaging; interim products obtained in the company during the production process; final products.

Each of the laboratories is located in detached, specially equipped for the purpose premises and has all necessary tools to carry out precise quality control and contemporary methods for analysis.

The equipment in the laboratories is continuously renewed and expanded by purchasing the most contemporary laboratory equipment from leading US manufacturers, and the staff systematically improves their qualification by learning new methods, participations in trainings and workshops in our country and abroad.

Activity

Transparent Labs USA operates in the following areas:

Manufacture of pharmaceutical preparations.

Dosing and packaging of active substances and excipients for extemporal and hospital use.
Contract manufacture and analysis of drugs. Contract manufacture and analysis of medicinal products for clinical trials.
Import, wholesale and distribution of raw materials for the chemical, pharmaceutical, cosmetic and food processing and packaging for pharmaceutical and cosmetic products.

Research & Development

- Development of technologies for medicinal products.
- Development and validation of analytical methods for active substances and excipients, and drug products.
- Preparation of dossiers for registration of medicinal products.
- GMP consultation and documentation.

Our Leadership Team

Transparent Labs USA is a company of enduring strength. We've been privileged to play a role in helping millions of people the world over be well and stay well through more than a century of change. As the science of human health and well-being has grown, we've been able to grow along with it. Even more important, we've helped shape and define what health and well-being means in everyday lives. Our products, services, ideas and giving now touch the lives of at least one billion people every day. We credit our strength and endurance to a consistent approach to managing our business, and to the character of our people.