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ISO Certificate Registration

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ISO Certificate Registration | ISO Registration | ISO 9001The ISO standard helps you develop a Quality Management System (QMS) to meet your customers’ quality requirements while continually improving operational processes. Since the standard is neither industry- nor product-specific, it may be used by any organization that provides a product or service.

The result of using ISO 9001 is shorter lead times, high delivery reliability, and consistently high quality of services and products, benefiting both your customers and your business.

Compliance to ISO 9001 will help you develop and optimize procedures and processes in your operations. You will be able to focus on what is important and save time and money, leaving you more competitive and better equipped to meet future challenges.

Whether you are a small business or a global corporation, ISO 9001 certification sends a clear message wherever you may do business. Certification increases confidence in your company, enhancing your competitiveness in all of the world’s local marketplaces.


 The ISO 14001 standard requires that a community or organization put in place and implement a series of practices and procedures that, when taken together, result in an environmental management system. ISO 14001 is not a technical standard and as such does not in any way replace technical requirements embodied in statutes or regulations. It also does not set prescribed standards of performance for organizations. The major requirements of an EMS under ISO 14001 include:

ISO Certificate Registration | ISO Registration | ISO 9001 |A policy statement which includes commitments to prevention of pollution, continual improvement of the EMS leading to improvements in overall environmental performance, and compliance with all applicable statutory and regulatory requirements.


ISO 45001 is an International Standard that identifies necessities for an occupational health and safety (OH&S) management system, with guidance for its use, to allow an organization to proactively progress its OH&S performance in avoiding damage and ill-health. ISO 45001 is intended to be applicable to any organization irrespective of its size, type and nature. ISO 45001 allows an organization, through its OH&S management system, to integrate other aspects of health and safety, like worker wellness/wellbeing; however, it should be noted that an organization can be compulsory by applicable legal necessities to also address such problems.

ISO 45001 certification was developed to mitigate any factors that can cause businesses and employees irreparable harm. Its standards are the result of great struggle by a committee of health and safety management specialists who looked closely at a number of other approaches to system management — including ISO 9001 and ISO 14001. In addition, ISO 45001 was designed to take other present occupational health and safety standards, like OHSAS 45001, into account — as well as the ILO’s labor standards, conventions and safety guidelines.


A GMP is a system for making sure that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

GMP is an abbreviation for Good Manufacturing Practices. GMP is an initiative of the WHO. The main aim of GMP is to see to it that the products are good sufficient for utilization after the final outcome. GMP governs the product at each and every step of manufacturing.

Good Manufacturing Practice (GMP) is that part of quality assurance which ensures that medicinal products are consistently produced and controlled to the quality standards appropriate to their intended use and as essential by the marketing authorization (MA) or product specification. GMP is concerned with both production and quality control.

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