A few words about us, our vision
The vision of Marseille Quincé laboratories is the production of high technology products for humans (pharmaceuticals, dietary supplements, medical technology, special nutrition and cosmetics) with studied action and safety, with respect to pharmaceutical science, having knowledge of pharmacy products.
To achieve this vision, the modern research and development unit of the laboratories is used as well as state of art production facilities that are harmonized with the European requirements and the protocols of good laboratory and production practice, as a result of which they meet the specifications of the quality certificates. The study of nature as well as the orientation to quality with modern techniques are interwoven in our mission.
Nature knows all the secrets and is waiting for us to discover them.
Production services
Support for Pharmaceuticals, Nutritional Supplements, Cosmetics, Medical Technology, Special Medical Purpose (FSMP).
Production Facilities
Manufacture of the product in our facilities, which guarantee the excellent quality of the products produced.
About the building installations: The construction of the recently completed building includes the control of temperature, air pressure and humidity throughout the laboratory installation.
About equipment: equipment used for production and packaging is threaded to control air production conditions.
All facilities are designed according to GMP (Good Manufacturing Practice) specifications.
The forms produced include liquid oral solutions and sprays as well as external forms such as creams, emulsions and gels manufactured on fully automatic production lines.
The daily capacity is 1.7TN per day.
Quality control
By Quality we generally mean the completeness of the characteristics of a product to meet constant needs, while by Quality Control / QC we mean the actions taken to achieve, support and improve Quality.
The laboratories are staffed with scientists and specially trained analysts, whose training is constantly enriched. QC carries out inspections at all stages of the production process, as well as product stability inspections throughout their life.
ELOT EN ISO 9001: 2015 ELOT EN ISO 13485: 2012 EN ISO 22716: 2007
Research and development
Product development tailored to the needs.
Specialized scientists are working to develop new products.
Their work includes: the selection of reliable suppliers of active substances, the formulation and production of batches of laboratory and industrial scale, the validation of the applied analytical methods and the conduct of stability studies.
The result of these actions is the creation of Technical Files in accordance with the European Directives.
Regulatory cases
Professionals in the field of regulatory affairs contribute significantly to the process of drug development and ensure the production of high quality files.
As the regulations and requirements for the approval of pharmaceutical products become more and more strict and strict, always with the aim of approaching the highest quality and ensuring public health, the Regulatory Affairs departments play an increasingly important role in the operation of Pharmaceutical Companies.
Environmental management
All our activities are carried out with the utmost respect for the environment and we continue to improve all our methods in this direction.
Even in our daily lives we take care of the proper use and management of recyclable materials.
Quality – Quality Assurance / QA
Quality in Rye Laboratories is ensured through QA (Quality Assurance), a system documented by a series of documents, which reflect the quality policy of our company. The Documentation System consists of the quality assurance manuals, the procedures and the instructions related to the work of the departments as well as the relevant forms.
The Quality Assurance System applied in our company is structured to combine the application of the rules of Good Manufacturing Practice (GMP’s) that govern the pharmaceutical industry and the application of the principles of the standards ISO 9001: 2015, ISO 13485: 2012, ISO 22716: 2007.
The implementation of the Quality Assurance System functions as an important control tool, able to add value to the produced result of daily work. Every stage of the process from the selection of raw materials to the production and storage of the final product, its promotion and distribution both in Greece and abroad, but also the development and approval of new products, are subject to strict controls, ensuring completeness. compliance with the high standards we have set.
Marseille Quincé Pharmaceutical Laboratories is committed to continuously improve the performance of the Assurance System
a) with the annual review of the implementation of the system by all the Directorates where the objectives and the returns of the previous year are evaluated and the goal setting of the new year is approved by the Management and
b) by implementing the annual program of internal inspections in all departments where the organization of the operation of the departments is checked and all the necessary measures are taken for the continuous improvement of their performance.
ELOT EN ISO 9001: 2015 ELOT EN ISO 13485: 2012 EN ISO 22716: 2007 EU GMP Manufacturing License
Contact Us
Marseille Quincé Universal Molecular Medicine (Group) Holding Ltd
Headquarter:
Room D2, 8/F
Phase 2, Hang Fung Industrial Building
2G Hok Yuen St
Hung Hom
Hong Kong
Hotline Enquiry: (852) 8494 3629
Email: info@marseille-quince.com
Branch-Europe:
Kalliorannatie 4, 21310 Vahto, Finland
Tel: +358 407434413
Fax: +358 22122200
