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OHSAS 18001 occupational health & safety

An occupational health and safety management system provides a framework for managing OHS responsibilities so they become more efficient and more integrated into overall business operations.

Health & Safety Policy

The main components of a health and safety policy fall under three heading.

  • The general policy statement, Organisation, Arrangements

Benefits of OHSAS 18001

  • Compliance with legislation
  • Ownership of Health and Safety Issues
  • Nominal effort is required
  • Training needs are identified and realised
  • Reduce Costs
  • Ongoing improvement
  • Liabilities minimised

ISO/IEC 27001:2013 is the international standard that describes best practice for an information security management system (ISMS). Accredited certification to ISO 27001 Certificate demonstrates that an organization is following global information safety best practices.
ISO IEC 27001 2013 is an information security management standard. It defines a set of information security management requirements. The official complete name of this standard is ISO/IEC 27001:2013 Information technology - Security techniques - Information security management systems - Needs. These needs can be found in the following seven sections:

Are You Losing Money Because You Don’t Know How CE Marking Certification Works?

The letters "CE" are the acronym of French phrase "Conformité Européene" which literally means "European Conformity". The term primarily used was "EC Mark" and it was formally replaced by "CE Marking" in the Directive 93/68/EEC in 1993. "CE Marking" is now used in all EU official documents.

Does my product need CE Marking?

CE Marking is most probably required if you export to the 27 European Union (EU) and 3 European Free Trade Association (EFTA) member states the following 20 groups of products -

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.

Muslims commonly use two terms to explain every subject as Halal or Haraam. Halal is a Arabic word which means allowable, lawful with respect to which no restriction exists, and the doing and consuming of which the Law-giver, Allah has permitted.

Halal means the opposite-unlawful that which the Lawgiver completely prohibited; anyone who engages in it is liable to incur the penalty of Allah in the Hereafter as well as a legal punishment in this world.

Halal in terms of food means that food must be:

  • Does not stem from or consists any part or item from animals that are forbidden (pig, carrion, having claws, talons or fangs, etc.) to Muslims by Islamic Law.
  • Food when prepared, processed, manufactured, packaged, stored or transported does not come in get in touch with or stored near any food that is forbidden and contain impurities as defined by Islamic Law.

What Is RoHS?

The definition and aim of the RoHS directive is quite simple. The RoHS directive aims to restrict certain dangerous substances commonly used in electronic and electronic equipment.RoHS is often referred to as the "lead-free directive," but it restricts the use of the following six substances:

  • Lead (Pb)
  • Mercury (Hg)
  • Cadmium (Cd)
  • Hexavalent chromium (Cr6+)
  • Polybrominated biphenyls (PBB)
  • Polybrominated diphenyl ether (PBDE)

When will the the directive be in effect and enforced?

As of July 1, 2006 all electronic and electrical products put on the European market must comply with EU Directive 2002/95/EC. There are no exceptions for pre-existing inventory which means that manufacturers products must be compliant before the July 1, 2006 cut off date.

Document Required for ISO Certificate

1, Company Registration Certificate Copy, 2. Company letterhead, 3. PRODUCT DETAILS, 4. GST Registration Copy, 5. I.D Proof of Authorised signatories

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