Validating the specifications, value, and safety of your raw materials, products, and assets.
CCI Services’ diverse range of inspection services can provide trusted support for your products, projects, and processes.
RoHS stands for Restriction of Hazardous Substances, and impacts the entire electronics industry and many electrical products as well. The original RoHS, also known as Directive 2002/95/EC, originated in the European Union in 2002 and restricts the use of six hazardous materials found in electrical and electronic products. All applicable products in the EU market since July 1, 2006, must pass RoHS compliance.
This industry-relevant Kosher certification process delivers a global solution that is practical to implement, and comparable in standard and quality to other recognized food schemes. It will help you to meet the demand for authentic and safe Kosher-certified food.
Halal is often used in reference to foods and drinks, i.e. foods that are permissible for Muslims to eat or drink under Islamic Sharjah (law). The criteria specifies both what foods are allowed, and how the food must be prepared. The foods addressed are mostly types of meat and animal tissue. The most common example of non-Halal (or Haraam) food is pork. Pork meat and its products cannot be eaten or used by Muslims at all due to historical, cultural, and hygienic concerns. Foods other than pork can also be Haraam.
In the vast landscape of industry and commerce, ensuring the safety and compliance of your products is of paramount importance, especially if you plan to introduce them to the European Economic Area (EEA). The CE Mark, short for "Conformité Européenne," serves as a prominent symbol of compliance with EU Product Safety Directives.
At CCI Product certification division ensures that your products are compliant with the region-specific regulations and standards in order to gain access to markets, commercialize your products and be able to compete.
Product certification activity is performed as a combination of evaluation of your products, process, and services, review, and final certification decision.
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any production that cannot be eliminated through testing the final product.
Good Storage Practice (GSP) is a system for ensuring that products are consistently produced and being stored ccording to national & international guideliness or standards. It is designed to minimize the risks involved in any food and pharmaceutical production that cannot be eliminated through testing the final product.
CGMP Certification confirms the product's identity, composition, quality, purity, and strength which they represent in the market. In the United States (US), Current Good Manufacturing (cGMP) Practices Regulated by the Food and Drug Administration (FDA) concerning the designing, monitoring, measuring, controlling, Processing, and maintenance of manufacturing processes, Operational environment, and infrastructure facilities.
GDPMD specifies the requirements for a quality management system to be established, implemented, and maintained by an established of medical device importer/distributor/ authorized representative to comply with the Malaysian Medical Device Act 2012 (Act 737) and Medical Device Regulations 2012.
Access our interactive ISO platform at app.companycertification.com As the trusted provider of your ISO certification, we offer entry to our online platform, where you can monitor the progress of your complete management system. This cloud-based platform is accessible to all users within your organization.
Effortlessly manage all your documentation, track tasks using project management tools, and record vital information using our extensive template library. Enjoy compliance, security, and unparalleled support—all included in the annual ISO certification fee! Access this comprehensive service now at app.companycertification.com.
