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Tax Consulting

Consulting Services

  • 1. Tax Consulting

    The methodology behind their approach is based on there being five core types of consultants within the consulting or advisory & management services industry.

  • 2. Management Consulting

    Many businesses now outsource their non-strategic activities or more complex tasks in order to access industry practice and cutting-edge technology.

  • 3. Financial Consulting

    Whether you’re a business or an individual preparing for the future, we can help you reach your goals through our best in class financial services & solutions.

  • 4. Human Resource Consulting

    Whether you’re a business or an individual preparing for the future, we can help you reach your goals through our best in class financial services & solutions.

  • 5. Property Consulting

    Whether you’re a business or an individual preparing for the future, we can help you reach your goals through our best in class financial services & solutions.

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Tax Consulting

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Income Tax
We Provide PAN Card, Filing of Income tax, TDS Returns, Consultancy on Income Tax Matters, Tax Refunds, Tax Planning & Savings, Maintenance of Income Tax Records, Liaisoning with Income Tax Authorities, Tax deduction account numbers.

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Sales Tax
We provide consultancy in Registration under VAT Act, Registration under CST Act, Online Filing of Returns, Rate of Tax under Delhi VAT Act, Consultancy of deposit of VAT, Consultancies on VAT and CST Act, Taxability of Sale of fixed assets, Objections, appeals.

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Service Tax
We Provide Service Tax Registration, Consultancy on Services and applicability of Service tax Act , Filing of Service Tax return in ST-3 ,Consultancy on deposit of monthly service tax of both corporate as well individuals, Maintenance of Service Tax Records, Liaisoning with respective Authority etc.

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Income Tax
We Provide PAN Card, Filing of Income tax, TDS Returns, Consultancy on Income Tax Matters, Tax Refunds, Tax Planning & Savings, Maintenance of Income Tax Records, Liaisoning with Income Tax Authorities, Tax deduction account numbers.

ROC Services | Popular ISO standards

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ISO 9001 : 2008
ISO 9001:2008 (QUALITY MANAGEMENT SYSTEM) – is the most widely recognized ISO standard. This is a basic quality management system that can be implemented in industries of any type, any size, anywhere in the world. Registration to ISO 9001:2008 Standard provides objective proof that a business has implemented an effective quality management system, and that it satisfies all of the requirements of the applicable ISO standard.

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ISO 14001:2004
ISO 14001:2004 (Environmental Management System) – is a global standard for environmental management systems which provides the framework for businesses to demonstrate their commitment to environmental responsibility. ISO 14001 is a product of the International Organization for Standardization (ISO). ISO 14001 is the world's first generic, internationally recognized standard for environmental management the goal of the ISO 14001 standard is to give the top management of any organization a framework for managing environmental impacts.

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ISO 22000:2005 / HACCP
ISO 22000 is an international standard designed to ensure worldwide safe food supply chains and provide a framework of internationally harmonised requirements for the global approach that is needed. A major resulting benefit is that ISO 22000 makes it easier for organisations to implement the Codex Alimentarius HACCP (Hazards Analysis and Critical Control Points) system for food hygiene in a harmonised way, which does not vary with the country or food product concerned. ISO 22000 allows all types of organisations within the food supply chain to implement a food safety management system. The supply chain members range from farms, feed producers, primary producers, food manufacturers, transport and storage operators and subcontractors to retail and food service outlets together with related business such as producers of equipment, packaging material, cleaning agents, additives and ingredients.

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OHSAS 18001:2007
OHSAS 18001 certification is an assessment specification for Occupational Health and Safety Management System certification. Since 1950, World Health Organization & International Labour Organization have defined the Occupational health & safety. In April 1999, the British Standard Institute released the specification that they called OHSAS 18001 certification. This was developed in response to strong worldwide demand for a generalized, comprehensive outline for managing occupational health & safety issues Occupational health should aim at.

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ISO 13485:2003
ISO 13485:2003 Certification Medical Devices - Quality Management System is an international standard that defines quality management system requirements for manufacturers of medical devices. ISO 13485:2003 certification contains requirements essential for organizations operating at any tier in the medical devices and pharmaceutical supply chain. The primary objective of the standard is to facilitate harmonized medical device regulatory requirements and as a result, it includes some particular requirements for manufacture, installation and servicing such as added requirements on record-control, sterilization and risk management.

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GMP
"Good manufacturing practice" or "GMP" are practices and the systems required to be adapted in pharmaceutical manufacturing, quality control, quality system covering the manufacture and testing of pharmaceuticals or drugs including active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidance that outline the aspects of production and testing that can impact the quality of a product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation. Basic concepts of all of these guidelines remain more or less similar to the ultimate goals of safeguarding the health of the patient as well as producing good quality medicine, medical devices or active pharmaceutical products. In the U.S. a drug may be deemed adulterated if it passes all of the specifications tests but is found to be manufactured in a condition which violates current good manufacturing guidelines. Therefore, complying with GMP is a mandatory aspect in pharmaceutical manufacturing.

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CE MARKETING
CE Marking The CE Mark certification is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives. The letters 'CE' are an abbreviation of Conformite Europeenne, French for European conformity. The CE Marking certification of products as "passport" which can allow a Manufacturer to freely circulate their products within the European market place.