History
The company was founded as an independent laboratory in 1982, performing quality control for the cosmetics industry and sterile material. In 1992 obtained the authorisation of the MINISTRY of Health to control pharmaceutical specialties and serves the pharmaceutical industry, working as a hired center for quality control departments, and development.
The center performs tests and biological determinations for the pharmaceutical, cosmetic, chemical, medical and surgical industrie. It is equipped with the necessary facilities and laboratories for studies of toxicity, pharmacology and microbiology.
It is approved and authorised by the Ministry of Health for the control of pharmaceutical products, cosmetics, medical devices, implants, toothpastes and the Ministry of Agriculture for the control of veterinary specialties.
Since 1998 when the company applied for inclusion in the program of compliance with Good Laboratory Practice (GLP), is certified in compliance with GLP (GLP) by the Directorate General of Health. Ministry of Health of the Community of Madrid), as set forth by the European Union and OECD.
Personnel
The experience of the working professionals: researchers, technicians and assistants is guaranteed by the long history of activity of the company and its capacity is backed by his scientific career and training. All those responsible for the analysis maintain a continuous communication with the client and keep absolute confidentiality on the conducted studies and the obtained results. Moreover, according to compliance with GLP standards there is a Quality Assurance Unit which oversees all critical phases studies and validates the results.
The laboratory is a research and analysis center that works closely with the industry within it operates, as well as with the administration that allows the firm to operate as a laboratory for quality control by contract or as a research center offering technical advice, implementation of new methods test and evaluation of new experimental models under development.
All methods are developed into standard operating procedures, and / or based on specific protocols approved between the involved parties.
Compliance with international standards of animal facilities and installation of GLP compliance allow Biolab to perform studies in experimental animals in safety ratings and research studies.
Facilities
The company has several animal housing and microbiology laboratories. The facilities and equipment are renewed periodically to adjust to the new regulations.
The animal facility installed in accordance with Directive (86/609 / EEC) is equipped with independent laboratories for different species, isolation rooms for special studies of medium or long term.
The department of microbiology separated and equipped to perform various processes laboratories; cleanroom, cell culture, microbiology laboratory, planting, sample preparation, etc.
Biolab develops a quality control in the laboratory at the highest level, understanding as such the verification of all the processes involved in the analysis and control of all the analyzed products.
Quality
Biolab brings quality to all aspects of the control process, from the reception of the sample, materials, equipment and culture media, to the analysis performed to all the products for the more than 100 clients that trust us. Including the work of all the technicians and managers who have adequate training for each position and job, and who watch at all times to ensure that all the quality standards for which we are accredited are met.
As a control laboratory with more than 30 years of experience in the pharmaceutical sector, we consider quality the basic pillar of the company, which has allowed us to advance and offer specialized advice adapted to the needs of our clients on the application of those regulations that are applicable to each particular product.
There is a Quality Assurance Unit which oversees all critical phases of studies and validates the results. Before each study a specific protocol for the product is established and a comprehensive report of the results is made once finished.
If someone requests that the study be certified under GLP standards, the Quality Assurance unit would audit in addition to the critical phases, all documentation related to the study to ensure that the GLP principles are closely followed.