Transparent Labs USA is an innovative, modern and dynamically developing pharmaceutical company.
The company was founded in 1995 in the city of Vineyard - USA. Members of the management team have academic backgrounds and solid experience in pharmaceutical and chemical engineering, research, development and clinical trials of medicines, as well as a deep understanding of people's needs for high-quality medical products and services.
The company has its own production facilities (buildings and equipment) and the necessary facilities, as well as a flexible organization of the workflow, which ensures 100% implementation of deliveries within the agreed time and volume.
Our ongoing goal is to improve the health of people by providing safe, clinically proven and effective medicines available to every patient. We guarantee patient safety in our products by using advanced technologies and systems, as well as high standards of Good Manufacturing Practices (GMP).
Quality assurance
The Transparent Labs USA quality assurance system covers all activities and aspects of the production and management cycles, as well as other activities related to their possible impact on the quality of products and services.
All functions and responsibilities related to quality assurance comply with the requirements of GMP (good manufacturing practice) and are specified in the relevant job descriptions, instructions, procedures and other service documents.
The quality assurance system covers all technological processes (from supply to distribution and after-sales service), as well as non-technological processes, with the aim of coordinating them and directing them towards the achievement of the company's ultimate goals - maintaining and developing the overall high quality of products. production and complete customer satisfaction.
Important aspects of a company's quality assurance system are:
- assessment and support of suppliers whose products and services comply with the company's policy for compliance with their stated management system requirements;
- current checks;
- the process of release of the final product;
- conducted checks and self-checks for all elements of GMP;
- systematic use of self-review reports and audits as a basis for developing and improving company policy.
Quality control at the enterprise is carried out in the analytical, chromatographic and microbiological laboratories, where highly specialized and highly qualified specialists work. It is noteworthy that Transparent Labs USA is one of the few drug manufacturing companies that has its own microbiological laboratory, which guarantees the microbiological purity of products.
Quality control applies to all without exception: received active substances; other raw materials, auxiliary materials, materials and packaging; intermediate products obtained in the company during the production process; end products.
Each of the laboratories is located in a separate, specially equipped room and has all the necessary equipment for precise quality control and modern methods of analysis.
The equipment in the laboratories is constantly updated and expanded through the purchase of the most modern laboratory equipment from leading US manufacturers, and the staff systematically improves their skills by studying new methods, participating in trainings and seminars in our country and abroad.
Research and development
- development of drug technologies;
- development and validation of methods for the analysis of active and excipients and drugs;
- preparation of a dossier for registration of medicines;
- consultations and documentation on GMP.