Business Certification

What is CE Marking (CE Mark)?
CE Marking is the symbol as shown on the top of this page. The letters “CE” are the abbreviation of French phrase “Conformité Européene” which literally means “European Conformity”. The term initially used was “EC Mark” and it was officially replaced by “CE Marking” in the Directive 93/68/EEC in 1993. “CE Marking” is now used in all EU official documents.
“CE Mark” is also in use, but it is NOT the official term. For instance, in the Directive 2007/47/ec, of 5 September 2007, amending the directives 90/385/eec, 93/42/eec & 98/8/ec, the term CE Marking appears 9 times whereas CE Mark appears nowhere in the entire 35-page document.
CE Marking on a product is a manufacturer’s declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislation, in practice by many of the so-called Product Directives.
*Product Directives contains the “essential requirements” and/or “performance levels” and “Harmonized Standards” to which the products must conform. Harmonized Standards are the technical specifications (European Standards or Harmonization Documents) which are established by several European standards agencies (CEN, CENELEC, etc).

Additional Information:

• Item Code: Ce
• Production Capacity: 10
• Delivery Time: 1 Day
• Packaging Details: Email & post

Additional Information:

• Item Code: 101
• Production Capacity: 10
• Delivery Time: 3
• Packaging Details: email

Additional Information:

• Production Capacity: 10
• Delivery Time: 3 Days
• Packaging Details: Email Id

Additional Information:

• Item Code: GMP02
• Production Capacity: 100
• Delivery Time: 1 DAY
• Packaging Details: BY EMAIL

1. Good manufacturing practice (GMP) is a concept that ensures products are consistently produced and controlled according to quality standards. It is designed to minimize the risks to the patient involved in any pharmaceutical production. GMP constitutes the license to operate in pharmaceutical manufacturing, and is a core condition worldwide. However, rules and interpretations differ from country to country and change frequently. Therefore, having fully trained experts at hand to help with the implementation of these rules is very important.
2. Costs reduced and resources saved. Evidence of safe and efficient food handling. Compliance with legal requirements and builds customer trust.
3. Fast & Hazel Free Process,
4. Best service at Best Price Guaranteed,
5. Certificate Valid Internationally,
6. Tender and Assistance on ISO Certification.

Additional Information:

• Item Code: GMP01
• Production Capacity: 100
• Delivery Time: 1 DAY
• Packaging Details: Email & Post

Additional Information:

• Item Code: 0101
• Production Capacity: 10
• Delivery Time: 3 Days
• Packaging Details: email copy

Additional Information:

• Item Code: ISO140012
• Production Capacity: 10
• Delivery Time: 3 DAYS

Learning Services outside Formal Education- Service Requirements for LSP (Learning Service Provider)

What is ISO 29990:2010 Certification

This standard specifies requirements for learning services outside formal education, including all types of life-long learning (e.g. vocational training and in-company training, either outsourced or in-house). These include any learning services provided by a learning service provider (LSP) that are addressed to learners themselves, as well as to sponsors who are acquiring the services on behalf of the learners. The key features of these kinds of services are that the goals of learning are defined and the services are evaluated, and that they involve interaction with the learner. The learning can be face-to-face, mediated by technology, or a blend of both.

In cases where the learning service provider is part of an organization that delivers products (i.e. goods and services) in addition to learning services, This standard only applies to learning services.

This standard is not aimed at schools, colleges and universities providing learning services as part of a formal education system, but it can be useful to them as a tool for reflection and self-evaluation.

Additional Information:

• Item Code: 29990
• Production Capacity: 10
• Delivery Time: 3 DAY

ISO 13485 is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 quality management standard series. ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. While ISO 13485 is based on the ISO 9001 process model concepts of Plan, Do, Check, Act, it is designed for regulatory compliance. Thus it is more prescriptive in nature and requires a more thoroughly documented quality management system.

ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose. A medical device organization can implement to help demonstrate compliance to laws and regulations of the medical device industry.

ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose.

Additional Information:

• Item Code: 13485
• Production Capacity: 10
• Delivery Time: 3

ISO 27001 is the international standard which is recognized globally for managing risks to the security of information you hold. Certification to ISO 27001 allows you to prove to your clients and other stakeholders that you are managing the security of your information. ISO 27001:2013 (the current version of ISO 27001) provides a set of standardized requirements for an Information Security Management System (ISMS). The standard adopts a process based approach for establishing, implementing, operating, monitoring, maintaining, and improving your ISMS.

ISO/IEC 27001, part of the growing ISO/IEC 27000 family of standards, is an Information Security Management System (ISMS) standard published in October 2013 by the International Organization for Standardization (ISO) and the International Electro technical Commission (IEC). Its full name is ISO/IEC 27001:2013 – Information technology — Security techniques — Information security management systems — Requirements but it is commonly known as “ISO 27001”.

ISO/IEC 27001 formally specifies a management system that is intended to bring information security under explicit management control

Additional Information:

• Item Code: 27001
• Production Capacity: 10

Additional Information:

• Item Code: 22000
• Production Capacity: 10
• Delivery Time: 3

Additional Information:

• Item Code: ISO29990
• Production Capacity: 100
• Delivery Time: 3 Days

Hazard Analysis and Critical Control Points(HACCP) is a management system used in the food industry and this chapter describes basic HACCP principles along with a few details from the more recent Hazard Analysis and Risk-Based Preventive Controls system variation.

The US Food and Drug administration created four food-specific websites describing important details for diary, juice, retail/food service, and seafood HACCP programs. These programs and efforts to teach how to control food risks will be discussed, including alleged violations of HACCP regulations, which are illustrated in food-related Warning Letters and publications citing needs for improved HACCP execution. Topics include information on hazards associated with juice and seafood, pest control, and drug residues in dairy products.

Additional Information:

• Item Code: haccp10
• Production Capacity: 10
• Delivery Time: 3
• Packaging Details: email

Additional Information:

• Item Code: 45001
• Production Capacity: 10
• Delivery Time: 3