Standards and Certifications
RJC COP / COC
Created in 2005, the RJC COPCoC certification aims to certify the best practices of companies that contribute to the gold or diamond supply chain, from the mine to the distribution. A company participating in the RJC initiative must obtain the certification issued by the RJC within two years of joining, and undertakes to implement and promote responsible practices in terms of ethics, the environment and working conditions.
Pibor is extremely proud to have obtained this RJC COP certification, which is supplemeted by another certification, the CoC standard, which guarantees responsible and non-conflict free procurement throughout the supply chain by means of a control chain composed of certified entities.
ISO9001: 2015
ISO 9001:2015 specifies the requirements for a quality management system. An organisation:
(a) must demonstrate its ability to consistently provide products and services that meet customer requirements and the applicable legal and regulatory requirements; and
(b) must strive to increase customer satisfaction through the effective application of the system, including processes for improving the system and ensuring compliance with customer requirements and the applicable legal and regulatory requirements.
All the requirements of ISO 9001:2015 are generic and are intended to apply to any organisation, regardless of its type or size or the products and services it provides.
ISO 13485:2016
ISO 13485:2016 sets out the requirements for a quality management system where an organization needs to demonstrate its ability to consistently provide medical devices and related services that meet customer and applicable regulatory requirements. These organisations may be involved in one or more stages of the life cycle including the design and development, production, storage and distribution, installation or associated services of a medical device, as well as the design, development or provision of associated activities (e.g. technical support).
Pibor ISO SA is your preferred partner in the fields of industrialisation and subcontracted manufacturing of microtechnical components for medical devices.
ISO 13485:2016 indicates that the company follows a procedure recognised by an independent body which audits it regularly in the field of Medical devices -- Quality management systems -- Requirements for regulatory purposes.
Reach
Pibor works in accordance with the REACH standard. The processes implemented ensure ongoing traceability of all components and quality control of the products manufactured in our company.
REACH: Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals. It came into effect on 1 June 2007.
REACH streamlines and improves the former European Union (EU) framework legislation on chemicals.
The main objectives of REACH are to ensure a high level of protection of human health and the environment against risks.
RoHS
RoHS stands for Restriction of the use of certain Hazardous Substances in electrical and electronic equipment.
This directive therefore applies to all new products placed on the market in the European Union, whether they are imported or manufactured in the Union.
MSST
MSST (CFST Directive 6508) refers to the mandatory development of a security system in companies/administrations and systematic prevention. The MSST method is primarily based on the employer's commitment to ensuring safe and healthy workplaces for its employees and its willingness to comply with the requirements on a daily basis.
We constantly implement internal actions and promote a policy of occupational risk prevention, in particular by enlisting occupational physicians and other occupational safety specialists (MSST).
The objective is to reduce the number of accidents and damage to health that cause intolerable suffering and places a heavy burden on the economy.