Services we provide

  • ISO 9001 (Quality Management System) 
  • ISO 14001 (Environmental Management System)
  • OHSAS 18001 (Occupational Health & Safety Management System)
  • ISO 45001 (Occupational Health and Safety)
  • ISO 50001 (Energy Management Systems)
  • ISO 22000 (Food Safety Management System)
  • ISO 27001 (Information Security Management System)
  • ISO 13485 (Medical Devices Management Systems)
Compliance Certificates
  • CE Marking
  • GMP (Goods Manufacturing Practices)

ISO 9001 QMS (Quality Management System)

All types of organizations can get benefitted by implementing ISO 9001:2015 standard as it is based on 8 principles

  • Customer Focus
  • Leadership
  • Involvement of people
  • Process approach
  • System approach towards management
  • Continual Improvement
  • Factual Approach to decision making
  • Mutual Beneficial Supplier Relations
 

ISO 14001 EMS (Environmental Management Systems)

It’s the principal management system standard which specifies the requirements for the formulation and maintenance of an EMS. There are three fundamental commitments required in an environmental policy that meets the requirements of ISO 14001 which are as follows

  • Prevention of Pollution
  • Compliance of legislation
  • Continual improvement of EMS
 

OHSAS 18001 (Occupational Health & Safety Management System)

The standard is applicable to any organization that wishes to eliminate or minimize risk to employees and other stakeholders who may be exposed to OH&S risks associated with its activities.

ISO 22000 FSMS (Food Safety Management System)

ISO 22000 is a truly international standard suitable for any business in the entire food chain, including inter-related organizations such as producers of equipment, packaging material, cleaning agents, additives and ingredients.

ISO 27001 ISMS (Information Security Management Systems)

ISO 27001 provides the framework for a technology neutral, vendor-neutral management system that enables an organization to assure itself that its information security measures are effective.

ISO 50001 EnMS (Energy Management Systems)

Standard is based on the management system model of continual improvement also used for other well-known standards such as ISO 9001 or ISO 14001. This makes it easier for organizations to integrate energy management into their overall efforts to improve quality and environmental management.

ISO 13485 (Medical Devices Management Systems)

Its primary objective is to facilitate harmonized medical device regulatory requirements.

ISO 13485 contains requirements that are essential for any organization operating at any tier in the medical device and pharmaceutical supply chain. It is especially relevant to manufacturers that wish to demonstrate applicable regulatory requirements, and by organizations whose services support medical device manufacturers.

What are the benefits of ISO registration?

  • International Acceptance
  • Effective Management Control
  • Marketing Advantage
  • Increased Customer Confidence
  • Employee satisfaction
  • Performance enhancement
  • Increased transparency and effectiveness of internal company process
  • Time and cost savings
  • Any size of organization can go for ISO certification
  • Improved product reliability
  • Better documentations of processes
  • Achieve company policy and goals
  • Better utilization of resources
  • Help monitor the effectiveness of your supply chain
  • Meet regulatory requirements
  • Improved ability to respond to Customer Requirements
  • Better working/High moral/Job satisfaction of employees

CE Marking

CE Mark is mandated by New Approach Directives. Many products are covered by these directives. To be placed on the market in the EU, it’s a legal requirement that some must bear CE marking. 

What is CE Marking?

The letters ‘CE’ on a product are the manufacturer’s claim that the product meets the requirements of all relevant European Directives.

CE marking on a product:

  • Indicates to governments that the product can be legally sold within the European Union (EU) and the European Free Trade Area (EFTA)
  • Ensures the product can move freely throughout the European Single Market
  • Indicates to customers that the product meets designated minimum safety standards and therefore a minimum level of quality
  • Promotes public health and safety
  • Enhances product credibility
  • Leads to improved sales and greater customer satisfaction

GMP (Good Manufacturing Practices)

We provide consultancy service for GMP WHO certification to our clients. GMP (Good Manufacturing Practices) is a standard defined by WHO (World Health Organization). GMP WHO certification ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization.