Empowering Success

ISO 9001 (Quality Management Systems)
specifies requirements for a quality management system when an organization:
a) Needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and
b) Aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.
All the requirements of ISO 9001 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.

ISO 14001 (Environment Management System)
An environmental management system helps organizations identify, manage, monitor and control their environmental issues in a “holistic” manner. It requires that an organization considers all environmental issues relevant to its operationsand resources’ use and efficiency.
This includes the need for continual improvement of an organization’s systems and approach to environmental concerns.


ISO 45001 (Occupational Health & Safety Management System)
The occupational health and safety (OH&S) management system, is a new international standard that provides a framework for an organization to manage risks and opportunities to help prevent work-related injury and ill health to workers. The intended outcome is to improve and provide a safe and healthy workplace. All of its requirements are designed to be integrated into an organization’s management and business processes.


ISO 22000 (Food Safety Management System)
Sets out the requirements for a food safety management system (FSMS) and can be certified to. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe.

Fassai (Food Safety and Standards Authority of India): We do the Basic, State and Central certification for Fassai. A food license by which is issued by the FSSAI is regarded as a permit which is required to operate a food-related business and also in order to ensure good quality of food in your business and for the benefits one from government actions on non-compliances.


ISO 20000 (Information Technology Service Management)
ISO 20000 is the international IT service management (ITSM) standard that enables IT organizations in-house, outsourced or external to ensure that their ITSM processes are aligned both with the needs of the business and with international best practice. Helps organizations benchmark how they deliver managed services, measure service levels and assess their performance.


ISO 27001 (Information Security Management System)
Is the international standard that describes the requirements for ISMS (information security management system). ISO 27001 is supported by its code of practice for information security management, ISO/IEC 27002:2013. Achieving accredited certification to ISO 27001 provides an independent, expert assessment that information security is managed in line with international best practice and business objectives.


ISO 13485 (Standard for Medical Devices)
Specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. This can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.


CE Marking
CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985.[1]The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States.
The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.


GMP (Good Manufacturing Practice)
A 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 pharmaceutical production that cannot be eliminated through testing the final product.


GDP (Good Distribution Practice)
Good distribution practices ensure maintaining product safety and quality during distribution across the supply chain and this practice is of significant importance for the pharmaceutical industry. Good Distribution Practices (GDP) Compliance report for Pharmaceutical Industry demonstrates Quality commitment & sound practices in the entire pharmaceutical distribution supply chain.


Firm Registration:
We do registration of firms (Individual, Partnership, Pvt. Ltd companies, LLP etc..) we help in getting the GST registration/PAN card.


MSME:
We help in getting the MSME certification to your organization.