This Standard recognizes technical proficiency and result validity of analytical laboratories.
The main target of this Standard is to define a Quality Management System to manufacture products that meet customer’s requirements.
ICSA validates computer systems based on the GDP (Good Development Practices) laws as stated by the EU.
GxP is based on the precepts for Good Pharmaceutical Industry Practices, covering all aspects from drug development to drug manufacturing.
We design a personalized plan to improve the processes of the laboratory increasing results and profits for our customers.
ICSA has over 15 years of experience as a consultancy for anaytical laboratories. Our main purpose is to offer solutions for laboratories. We work with chemical laboratories, environmental laboratories, physical laboratories and many other types of analytical laboratories. ICSA has developed a well-structured methodology to implement the ISO standards correctly.
“Hacer del trabajo la mayor motivación.”
Quality Manager & Quality Systems Consultant
Graduate in Bussiness Management – MBA
“Si no conozco una cosa, la investigaré.”
Quality Systems Consultant
PhD in Chemistry
All ISO standards of quality management such as ISO 9001, ISO 17025, ISO 14001, etc. emphasize the importance of measuring and monitoring the situation of the enterprises compared to the requirements of the implemented quality management system.
UNE-EN ISO/IEC 17025 standard establishes requirements to recognize technical proficiency and result validity of the laboratories.
ISO/IEC 17043 standard provides the foundations to determine the proficiency of the intercomparison programs of supplier organizations. Laboratories and accreditation entities could use the results of the intercomparison programs for the accreditation process if they can trust the correct operation of these programs.
Testqual SEIMC
ISO 22716 standard provides guidelines of Cosmetic Products Good Manufacturing Practices (GMP’s) for the production, control, storage and distribution of these products.
Cosmetic Products Manufacturers
Cosmetic Ingredients Manufacturers
Cosmetic Containers Manufacturers
Pharmaceutical laboratories
UNE-EN ISO 9001 standard’s main target is to increase the customer’s satisfaction, including processes for continuous improvement and the assurence of conformity of the products.
UNE-EN ISO 14001 standard establishes the requirements for an environmental management system. This system allows the organization to develop and implement a policy and goals based on the significant aspects of their activities.
RIIA
Tecda Control
GxP’s main target is to ensure and certify that a product meets the safety standards and its operating instructions. GxP’s main aspects:
Pharmaceutical Industry
ICSA validates computer systems based on the GDP laws as stated by the EU. The final report contains:
The main target of this validation is to demonstrate and certify that the system is strong, effective and safe.
Pharmaceutical Industry