Third Party Inspection

We offer comprehensive third party assessment, inspection and quality assurance services including Factory Audits, OEM Development, Raw Material Inspection, Initial Production Check, In-Production Check, Random Inspection and Loading Supervision. Our third party assessments are impartial therefore provide credible basis for verification for diverse organizations.

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CE Marking

Existing in its present form since 1993, the CE marking is a key indicator of a product's compliance with EU Legislation and enables the free movement of products within the European market. By affixing the CE marking on a product, a manufacturer is declaring, at their sole responsibility, conformity with all of the legal requirements to achieve CE marking and therefore ensuring validity for that product to be sold throughout the European Economic Area. This also applies to products made in third countries which are sold in the EEA.

CE marking does not indicate that a product was made in the EEA, but states only that the product has been assessed before being placed on the market and thus satisfies the legislative requirements. It means that the manufacturer has verified that the product complies with all relevant essential requirements (such as safety, health, environmental protection requirements) of the applicable directive(s) or, if stipulated in the directive(s), has had it examined by a notified conformity assessment body.

However, not all products must bear the CE marking. Only those product categories subject to specific directives that provide for the CE marking are required to be CE-marked. CE-marked products are bought not only by professionals (e.g. medical devices, lifts, machinery and measuring equipment) but also by consumers (e.g. toys, PCs, mobile phones and light bulbs).

The CE marking is a kind of trade passport for the European marketplace: it allows the manufacturer to freely circulate their product throughout the 30 countries of the European Economic Area (EEA).

Benefits of CE Marking:-

  • It indicates a product's conformity with the "essential requirements" of the directives.
  • Allows products to be placed in the European market.
  • Ensure the free movement of goods.
  • Allows the withdrawal of non-conforming products by customs and enforcement authorities.

Training Programmes

  • To bring the positive change in the individual & the organisation to help them to reach out their goals by providing them with quality inputs in the multi discipline programme conducted by PIS.
  • To make the individuals excel in a unique way in their life.
  • Motivates human with quality inputs.
Training Details:-
  • ISO 9001 Lead Auditor Course Management System Training.
  • ISO 14000 Environment Management System Training.
  • ISO 22000 International Food Management System Training.
  • OHSAS 18001 Occupational Health & Safety Management System Training.
  • ISO 27000 Information Security Management System Training.
  • ISO 9000 Quality Management System Training.