ISO CERTIFICATION

Chiman S.r.l. is a third-party laboratory, founded in 1991, specializing in performing chemical and chemical-physical analyses for the pharmaceutical sector, performing analytical activities on clients’ proprietary products and/or samples according to protocols established/approved by them and performing analyses relevant for GMP purposes or for exploratory R&D purposes.
Chiman is focused on improving global health, with over 25 years of experience in pharmaceutical development and testing. This is achieved by providing a portfolio of analytical and bioanalytical services that help customers transform scientific discoveries into new medicines.
Chiman has a strong commitment to Environmental Protection, Worker Health and Safety, Energy Efficiency and Environmental Sustainability in all aspects of its service delivery, aiming to continuously improve service, customer satisfaction and the achievement and maintenance of high quality standards in the various areas of interest.
Our mission is to provide high-quality customized services to pharmaceutical companies with a view to increasing the sustainability of their processes.
Our key asset is flexibility: not only do we work to make the customer’s vision our vision, but we aspire to become a partner in their projects.
We focus on analytical chemistry, biochemistry and medical devices, with expertise in both raw materials and conventional finished products as well as significant experience in the respiratory therapeutic area, combining analytical leadership, innovative technology and scientific expertise in the field to provide a state-of-the-art service for both customers and patients.

We perform a wide range of services, including:

analysis of inhalation preparations
conventional formulations
generic drugs
development studies
biological analyses
stability and preservation tests
identification of impurities/degradation products
analysis for batch release for retail sale on the market
analyses for batch release for clinical studies

Chiman S.r.l. has been authorized by AIFA to perform chemical-physical controls on medicinal products for human use since July 2006 and on experimental medicinal products since December 2008.

Chiman is authorized by AIFA to carry out chemical (F1) and chemical-physical (F2) controls on medicinal products for human use and on investigational medicinal products for clinical trials pursuant to Legislative Decree of 24 April 2006, No. 219 as amended.

Chiman is FDA registered (FEI Number: 3015176596).

‘Chiman aims to make a concrete contribution to the health and improvement of people’s quality of life while respecting its Workers and the Environment also through energy efficiency’.

Fundamental points of this policy are:

the commitment to guarantee the availability of the information and resources necessary to achieve the objectives and targets set in terms of the Environment, Workers’ Health and Safety as well as Energy Efficiency and environmental sustainability of activities;
the commitment to comply with all the mandatory regulations applicable to the activities of Chiman s.r.l. concerning the Environment, Workers’ Health and Safety and Energy use;
the commitment to ‘maintaining the level of Effectiveness’ of the Quality Management System, of the Environment, Health, Safety and Energy Integrated Management System, of what is defined in the respective Policies and the related Objectives with a view to ‘Continuous Improvement
the commitment to periodically review the Quality Management System, the Environment, Health, Safety and Energy Integrated Management System, the related Policies and Objectives with a view to ‘Continuous Improvement
the commitment to the protection of the Environment, to the prevention of pollution and to increasing environmental sustainability;
the commitment to provide safe and healthy working conditions for the prevention of accidents and occupational diseases, eliminating risks to Workers’ Health and Safety and, where not possible, reducing them through appropriate prevention and protection measures;
the commitment to involve Workers and their representatives through specific consultation and participation activities;
support the procurement of energy-efficient products and services that have an impact on energy performance, while keeping the level of quality as high as possible;
support design activities that consider improving energy performance;
the commitment to identify, recognize, pursue and satisfy the needs of ‘Interested Parties’ at a Local, Regional, National, European and Global level;
the commitment to promote, pursue and periodically verify the satisfaction of Customers who use Chiman’s Services;
the active participation in the continuous improvement of the quality of the Services by all the Personnel involved, including external suppliers and collaborators;
the creation of an internal climate marked by collaboration and optimization of the capabilities and satisfaction of all Collaborators;
attention to Environmental, Energy and Safety issues in the workplace.
the attention and active participation in the increase of the ‘Italian Product’ image in Europe and worldwide;
attention to Ethical and Social components in all operational phases, namely
- - in relations with production and employment realities;
  - in relations with the ‘market’;
  - in the traceability and utilization of Skills and Research itself for emancipatory and social purposes;
  - in respecting multi-ethnicity and religious and areligious pluralism as essential values for socio-cultural growth;
  - in the employment of social issues through the pursuit of objectives for the development of employment opportunities.