We are the prominent Service Provider of Trademark Registration in India. Our Trademark Registration Services are highly praised by the clients for their timeliness and authenticity. The Trademark Registration Services, we offer, help the firms in providing undiminished edge over competitors by properly addressing the best solutions at reasonable rates to the valued clients.

Your trade mark can be a valuable business asset. Trade marks have come to represent not only actual goods and services, but also the reputation of the business. Some companies spend millions nurturing their corporate identities. Companies like Michelin, Levi Strauss and Intel consider their trade marks their most valuable assets? The President of Coca-Cola stated that the corporation's buildings, machinery, equipment, vehicles and physical property could all be destroyed, but that the business would have no trouble getting back on its feet, provided the trade mark survived.

What is a trademark  ?

Trademarks are concerned with brand identity - they can be distinctive words, marks or other features, the purpose of which is to establish, in the mind of the customer, a link between the particular products or services and the company. A trade mark is a sign by which a business identifies its products or services and distinguishes them from those supplied by competitors.

A trademark can be any word (PEPSI), name (TATA), symbol or device (Microsoft), slogan (Yeh Pyas Hai Badi & Thanda Matlab Coca Cola), package design (Coca-Cola bottle) or combination of these that serves to identify and distinguishes a specific product from others in the market place or in trade. Even a sound (Britania chimes) color combination, smell or hologram can be a trademark under some circumstances. The term trademark is often used interchangeably to identify a trademark or service mark.

What can be registered as Trademarks?

Any sign capable of being represented graphically. Thus marks may be one or a combination of words (including slogans), letters, and numerals. They may consist of drawings, symbols, three-dimensional signs such as shape and packaging of goods, audible signs such as music or vocal sounds, fragrances, or colours. Generally, trade marks are protected for specific classes of products and services for periods of 10 years, renewable indefinitely.

What are the requirements for registering a trade mark?

• Your trade mark must be distinctive meaning that a customer seeing the mark can immediately link the goods or services to a particular manufacturer/ supplier. Thus commonly used words are generally not acceptable except in a slogan.
• Your trade mark must not be deceptive. It must not be such that it would deceive the public as to the geographical origin or to the nature, quality, or other characteristics of the product or service.
• Your trade mark must not be descriptive. It cannot describe the product or service.
• Your trade mark must not belong to the exclusions provided by the law e.g. photographs, drawings or names of people or places unless they can be shown to be particularly distinctive.
• Your trade mark must be in conformity with public order and morality. Remember that registration of a company name, a business name or a domain name is not the same as registering a trade mark. The requirements are different.

We are highly professional in serving Company Registration Services to the respected clients. Our team of experts firstly understands the varied needs of the clients and then evaluates them on the industry parameters to analyze the actual problem or demand. Further, as per the set industry guideline they assist the clients and then serve them with the best solution at reasonable prices.

We are engaged in formation/registration of the following two types of companies as per Companies Act, 1956

• Private Limited Company.

• Public Limited Company

Differences Between Private Limited Company And Public Limited Company :

Distinction Between A Public Company And a Private Company Following are the main points of difference between a Public Company and a Private Company :

• Minimum Paid-up Capital

• Minimum number of members required to form a private company is 2, whereas a Public Company requires atleast 7 members. Maximum number of members

• Maximum number of members

• in a Private Company is restricted to 50, there is no restriction of maximum number of members in a Public Company.

• Transerferability of shares

• There is complete restriction on the transferability of the shares of a Private Company through its Articles of Association , whereas there is no restriction on the transferability of the shares of a Public company.

• Issue of Prospectus

• A Private Company is prohibited from inviting the public for subscription of its shares, i.e. a Private Company cannot issue Prospectus, whereas a Public Company is free to invite public for subscription i.e., a Public Company can issue a Prospectus.

• Number of Directors

• A Private Company may have 2 directors to manage the affairs of the company, whereas a Public Company must have atleast 3 directors.

• Consent of the directors

• There is no need to give the consent by the directors of a Private Company, whereas the Directors of a Public Company must have file with the Registrar a consent to act as Director of the company.

• Qualification shares

• The Directors of a Private Company need not sign an undertaking to acquire the qualification shares, whereas the Directors of a Public Company are required to sign an undertaking to acquire the qualification shares of the public Company .

• Commencement of Business

• A Private Company can commence its business immediately after its incorporation, whereas a Private Company cannot start its business until a Certificate to commencement of business is issued to it.

• Shares Warrants

• A Private Company cannot issue Share Warrants against its fully paid shares, Whereas a Private Company can issue Share Warrants against its fully paid up shares.

• Further issue of shares

• A Private Company need not offer the further issue of shares to its existing share holders, whereas a Public Company has to offer the further issue of shares to its existing share holders as right shares. Further issue of shares can only be offer to the general public with the approval of the existing share holders in the general meeting of the share holders only.

• Statutory meeting

• A Private Company has no obligation to call the Statutory Meeting of the member, whereas of Public Company must call its statutory Meeting and file Statutory Report with the Register of Companies.

Details & Documents Required For New Company Incorporation as below :

• Name of The Company (with the six-option name)

• Registered Address of the Company

• Full Name of the Directors

• Fathers Full Name of the Directors

• Residential Address of the Directors

• Date of Birth the Directors

• 3nos. of latest Passport Size Photographs of the Directors

• Address Proof of The Directors (i.e. Copy of Ration Card, Passport, latest Electricity Bill, Telephone Bill, etc)

• Identity Proof of the Directors (i.e. Voting Card, Driving Licence, School Leaving Certificate, etc)

• If the Din number of the Director is approve, then kindly provide us din number.

We are widely acknowledged in this industry for providing highly efficient CE Marking Certification Services. The CE Marking Certification Services, we provide, are highly acclaimed among the clients for the reliability and confidentiality. We provide these CE Marking Certification Services at the reasonable rates to the clients without consuming much of their time.

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. The CE Marking certification declares that your product complies with the Essential Requirements of the applicable EU Directives. Applicable requirements are set forth in various European Directives that replace individual country safety standards. The Directives apply to products manufactured within but also exported to the European Union.The CE Mark certification is placed on a product as the manufacturer’s visual identifier that the product meets the requirements of relevant European Directives. It is mandatory for a wide range of products sold within or exported to the European market.

To facilitate free trade and ensure the safety of certain products, European countries have developed a series of standards, or Directives as they are called. Compliance is mandatory. It is a legal obligation on the part of the manufacturer or his agent. Penalties for failing to get CE-Marking certification for a product can be severe.
If you wish to sell your products within the European Union member states and the European Economic Area, the product in question must comply with the Directive(s). This also applies if you are a manufacturer who wants to export products into the European Member countries.

The Directives replace individual country standards as they relate principally to the safety of these products.

• pressure equipment
• machinery of almost any description
• electrical and electronic equipment
• medical devices and equipment
• personal protective equipment
• Equipment for use in potentially explosive environments
• Determine which, if any, EU Directives apply to your product(s),
• Determine the extent to which your product already complies with the essential requirements of the Directives.
• Choose conformity assessment routes. Depending on the nature of the equipment or product, you may be able to implement and declare compliance and affix the CE mark certification without assistance or service from an external company.

A Notified Body is an independent body appointed by an agency within one of the European countries, usually governmental, as being capable of performing the duties of a Notified Body as defined by the Directives.

The company is considered as a reliable Service Provider of ISO Certification. Under ISO Certification Services, we provide Phase of documentation, Pre-Certification Audit (optional), Certification audit, and Certificate Granting and Surveillance Audits Services to the clients. The clients, associated with us, highly praise us for providing the best solution at reasonable rates within defined timeframe.

What is a ISO Certification?

ISO is the family of standards for quality management system. ISO 9000 is maintained by ISO, the International Organisation for Standardization and is administered by accreditation and certification bodies. The rules are updated, as the requirements motivate changes over time. Some of the requirements in ISO 9001:2008 (which is one of the standards in the ISO 9000 family) include :

• A set of procedures that cover all key processes in the business.
• Monitoring processes to ensure they are effective.
• Keeping adequate records.
• Checking output for defects, with appropriate and corrective action where necessary.
• Regularly reviewing individual processes and the quality system itself for effectiveness
• facilitating continual improvement

A company or organization that has been independently audited and certified to be in conformance with ISO 9001 may publicly state that it is "ISO 9001 certified" or "ISO 9001 registered". Certification to an ISO 9001 standard does not guarantee any quality of end products and services; rather, it certifies that formalized business processes are being applied.

IQM :

International Quality Management (IQM) is providing ISO Accredited ISO 9001, ISO 14001, OHSAS 18001, HACCP, ISO 22000, ISO 13845, ISO/TS -16949, ISO 29990 & ISO 50001 Certification Services from UASL and ASCB (UK). UASL and ASCB (UK) are the independent and impartial Accreditation’s Board from UK.

Certification procedure :

• In the case of interest for certification of your management system, the procedure is very simple :

  • Complete an Application for Certification form (AfC)

  • On the base of AfC we will process project of the Price Offer (PO)

  • After the acceptation (ratification) of the Price Offer from your side we will prepare a draft of the Contract

  • After the ratification of the Contract by negotiators this Contract comes into force and it becomes legally binding – Contract is signed for 3 years (the validity of an certificate is also 3 years)

  • Within the 3 years’ validity of Contract we conduct 1 certification audit and 2 surveillance audits (vide infra)

• A process of management system certification has these basic phases:

  • Phase of audit planning

  • Assessment of documentation

  • Pre-certification audit (optional)

  • Certification audit

  • Certificate granting and surveillance audits

Phase of audit planning  :

Phase of an audit planning represents planning of an audit. Chief of auditors nominates a lead auditor, an auditor and a specialist from examination scope. Audit team responds to qualified performed audit.

Assessment of management system documentation :

Documentation assessment is performed for the scope of accessory information for planning of a management system certification audit and of monitoring, that there were established basic requirements for proper working of a management system. An auditee is asked to present a quality manual and other reference documentation regarding to standard requirements, according to which the system will have been certified at least 14 days before the audit performance.

Pre-certification audit(optional) :

Pre-audit is performed in the location of a customer with the aim of nonconformities elimination, which can exist in a management system of an auditee. The certification audit is performed in the location of a customer and in the individual working places, which are the object of assessment, according to a customer requests scheduled in the contract. The audit process performance has got these phases :

• Planning (program) – lead auditor determines the timetable with requests for the attendance of individual authorized persons.
• Performance – this stage represents the proper audit performance.
• Completion – team of auditors evaluates the audit performance at the final negotiation with the management representatives of the audited company, the team of auditors assesses dates for elimination of recognized nonconformities.
• Evaluation – the final document of a certification audit is the Certification Audit Report. A Lead auditor prepares a report; he is also responsible for its correctness and completeness. A lead auditor is assessable to add comments of auditors and specialists, who actively took part in an audit, after the personal consultation with them to the report. Certification granting and surveillance audits. If a director of certification body does not find out any significant facts, which should resist to assignments of a lead auditor established in the certification audit report a director of certification body publishes positive consideration with the consideration of a lead auditor and grants a certificate.

The Product Certification Services, provided by us, are widely praised amongst the clients due to high reliability and timeliness. Under Product Certification Services, we provide Services for certain products that have passed performance tests and quality assurance tests requirements stipulated in contracts, regulations, or specifications. Besides, our team of experts caters these Product Certification Services within stipulated time frame as per the requirements of the valued clients.

Product certification or product qualification is the process of verifying that a certain product has passed performance tests and quality assurance tests or qualification requirements stipulated in contracts, regulations, or specifications. For example, it may relate to a building code, nationally accredited test standards, or a set of regulations governing quality and minimum performance requirements. Certifications (and the certificates that document their existence) are often called certs in the everyday jargon of various industries.

ISI Mark (Indian Standards Institution ) :

Formulation of Indian Standards for products and services by bringing together and coordinating various interest groups like manufacturers, consumers, technical experts, testing personnel and others interested. The standards so prepared are known as Indian Standards (IS) and are considered as legal documents. The first Indian Standard formulated was for the National Flag (IS 1). So far BIS has published about 18000 Indian Standards covering various products, codes of practices, terminology, etc for various industrial and economic sectors. The Indian Standards are used not only by the industry but also by the Government, students, consumers and regulatory authorities. The standards are priced publications and are available from all the offices of the Bureau.

CE Marking :

Sai IP Consult Solutions provides support to medical device companies that are seeking CE regulatory approval for their products in Europe. Saiipconsult consultants have a wealth of experience in the preparation of regulatory submissions required to obtain CE marketing clearance and have built strong relationships with the Notified Bodies. Qserve can help you bring your product to the market faster, minimizing the time and costs involved, and maximizing your product revenues.

"CE Mark" means that the product is safe and fit for the purpose for which it was made. Medical Devices Directives (MDD) specify requirements which must be met before permission is granted to apply the CE marking to your medical device and placing it on the market. The Directives which apply to medical devices are :

• Active Implantable Medical Device Directive (90/385/EEC) : This directive covers all medical devices, which rely on a power supply to function and that are left in the human body. These include implantable cardiac pacemakers, implantable nerve stimulators, etc

• Medical Device Directive (93/42/EEC) : The Medical Device Directive covers most other medical devices (active and non-active) and their accessories that are not covered by the first or the third directive. This concerns a large number of products ranging from walking aids to prosthetic heart valves.

• In Vitro Diagnostic Medical Device Directive (98/79/EC) : The In Vitro Diagnostic Medical Device Directive will cover any reagent, reagent product, control material, kit, medical device, instrument, apparatus or system which is intended to be used in-vitro for the examination of substances derived from the human body

We are the prominent Service Provider of Trademark Registration in India. Our Trademark Registration Services are highly praised by the clients for their timeliness and authenticity. The Trademark Registration Services, we offer, help the firms in providing undiminished edge over competitors by properly addressing the best solutions at reasonable rates to the valued clients.

Your trade mark can be a valuable business asset. Trade marks have come to represent not only actual goods and services, but also the reputation of the business. Some companies spend millions nurturing their corporate identities. Companies like Michelin, Levi Strauss and Intel consider their trade marks their most valuable assets? The President of Coca-Cola stated that the corporation's buildings, machinery, equipment, vehicles and physical property could all be destroyed, but that the business would have no trouble getting back on its feet, provided the trade mark survived.

What is a trademark  ?

Trademarks are concerned with brand identity - they can be distinctive words, marks or other features, the purpose of which is to establish, in the mind of the customer, a link between the particular products or services and the company. A trade mark is a sign by which a business identifies its products or services and distinguishes them from those supplied by competitors.

A trademark can be any word (PEPSI), name (TATA), symbol or device (Microsoft), slogan (Yeh Pyas Hai Badi & Thanda Matlab Coca Cola), package design (Coca-Cola bottle) or combination of these that serves to identify and distinguishes a specific product from others in the market place or in trade. Even a sound (Britania chimes) color combination, smell or hologram can be a trademark under some circumstances. The term trademark is often used interchangeably to identify a trademark or service mark.

What can be registered as Trademarks?

Any sign capable of being represented graphically. Thus marks may be one or a combination of words (including slogans), letters, and numerals. They may consist of drawings, symbols, three-dimensional signs such as shape and packaging of goods, audible signs such as music or vocal sounds, fragrances, or colours. Generally, trade marks are protected for specific classes of products and services for periods of 10 years, renewable indefinitely.

What are the requirements for registering a trade mark?

• Your trade mark must be distinctive meaning that a customer seeing the mark can immediately link the goods or services to a particular manufacturer/ supplier. Thus commonly used words are generally not acceptable except in a slogan.
• Your trade mark must not be deceptive. It must not be such that it would deceive the public as to the geographical origin or to the nature, quality, or other characteristics of the product or service.
• Your trade mark must not be descriptive. It cannot describe the product or service.
• Your trade mark must not belong to the exclusions provided by the law e.g. photographs, drawings or names of people or places unless they can be shown to be particularly distinctive.
• Your trade mark must be in conformity with public order and morality. Remember that registration of a company name, a business name or a domain name is not the same as registering a trade mark. The requirements are different.

We are highly professional in serving Company Registration Services to the respected clients. Our team of experts firstly understands the varied needs of the clients and then evaluates them on the industry parameters to analyze the actual problem or demand. Further, as per the set industry guideline they assist the clients and then serve them with the best solution at reasonable prices.

We are engaged in formation/registration of the following two types of companies as per Companies Act, 1956

• Private Limited Company.

• Public Limited Company

Differences Between Private Limited Company And Public Limited Company :

Distinction Between A Public Company And a Private Company Following are the main points of difference between a Public Company and a Private Company :

• Minimum Paid-up Capital

• Minimum number of members required to form a private company is 2, whereas a Public Company requires atleast 7 members. Maximum number of members

• Maximum number of members

• in a Private Company is restricted to 50, there is no restriction of maximum number of members in a Public Company.

• Transerferability of shares

• There is complete restriction on the transferability of the shares of a Private Company through its Articles of Association , whereas there is no restriction on the transferability of the shares of a Public company.

• Issue of Prospectus

• A Private Company is prohibited from inviting the public for subscription of its shares, i.e. a Private Company cannot issue Prospectus, whereas a Public Company is free to invite public for subscription i.e., a Public Company can issue a Prospectus.

• Number of Directors

• A Private Company may have 2 directors to manage the affairs of the company, whereas a Public Company must have atleast 3 directors.

• Consent of the directors

• There is no need to give the consent by the directors of a Private Company, whereas the Directors of a Public Company must have file with the Registrar a consent to act as Director of the company.

• Qualification shares

• The Directors of a Private Company need not sign an undertaking to acquire the qualification shares, whereas the Directors of a Public Company are required to sign an undertaking to acquire the qualification shares of the public Company .

• Commencement of Business

• A Private Company can commence its business immediately after its incorporation, whereas a Private Company cannot start its business until a Certificate to commencement of business is issued to it.

• Shares Warrants

• A Private Company cannot issue Share Warrants against its fully paid shares, Whereas a Private Company can issue Share Warrants against its fully paid up shares.

• Further issue of shares

• A Private Company need not offer the further issue of shares to its existing share holders, whereas a Public Company has to offer the further issue of shares to its existing share holders as right shares. Further issue of shares can only be offer to the general public with the approval of the existing share holders in the general meeting of the share holders only.

• Statutory meeting

• A Private Company has no obligation to call the Statutory Meeting of the member, whereas of Public Company must call its statutory Meeting and file Statutory Report with the Register of Companies.

Details & Documents Required For New Company Incorporation as below :

• Name of The Company (with the six-option name)

• Registered Address of the Company

• Full Name of the Directors

• Fathers Full Name of the Directors

• Residential Address of the Directors

• Date of Birth the Directors

• 3nos. of latest Passport Size Photographs of the Directors

• Address Proof of The Directors (i.e. Copy of Ration Card, Passport, latest Electricity Bill, Telephone Bill, etc)

• Identity Proof of the Directors (i.e. Voting Card, Driving Licence, School Leaving Certificate, etc)

• If the Din number of the Director is approve, then kindly provide us din number.

We are widely acknowledged in this industry for providing highly efficient CE Marking Certification Services. The CE Marking Certification Services, we provide, are highly acclaimed among the clients for the reliability and confidentiality. We provide these CE Marking Certification Services at the reasonable rates to the clients without consuming much of their time.

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. The CE Marking certification declares that your product complies with the Essential Requirements of the applicable EU Directives. Applicable requirements are set forth in various European Directives that replace individual country safety standards. The Directives apply to products manufactured within but also exported to the European Union.The CE Mark certification is placed on a product as the manufacturer’s visual identifier that the product meets the requirements of relevant European Directives. It is mandatory for a wide range of products sold within or exported to the European market.

To facilitate free trade and ensure the safety of certain products, European countries have developed a series of standards, or Directives as they are called. Compliance is mandatory. It is a legal obligation on the part of the manufacturer or his agent. Penalties for failing to get CE-Marking certification for a product can be severe.
If you wish to sell your products within the European Union member states and the European Economic Area, the product in question must comply with the Directive(s). This also applies if you are a manufacturer who wants to export products into the European Member countries.

The Directives replace individual country standards as they relate principally to the safety of these products.

• pressure equipment
• machinery of almost any description
• electrical and electronic equipment
• medical devices and equipment
• personal protective equipment
• Equipment for use in potentially explosive environments
• Determine which, if any, EU Directives apply to your product(s),
• Determine the extent to which your product already complies with the essential requirements of the Directives.
• Choose conformity assessment routes. Depending on the nature of the equipment or product, you may be able to implement and declare compliance and affix the CE mark certification without assistance or service from an external company.

A Notified Body is an independent body appointed by an agency within one of the European countries, usually governmental, as being capable of performing the duties of a Notified Body as defined by the Directives.

The company is considered as a reliable Service Provider of ISO Certification. Under ISO Certification Services, we provide Phase of documentation, Pre-Certification Audit (optional), Certification audit, and Certificate Granting and Surveillance Audits Services to the clients. The clients, associated with us, highly praise us for providing the best solution at reasonable rates within defined timeframe.

What is a ISO Certification?

ISO is the family of standards for quality management system. ISO 9000 is maintained by ISO, the International Organisation for Standardization and is administered by accreditation and certification bodies. The rules are updated, as the requirements motivate changes over time. Some of the requirements in ISO 9001:2008 (which is one of the standards in the ISO 9000 family) include :

• A set of procedures that cover all key processes in the business.
• Monitoring processes to ensure they are effective.
• Keeping adequate records.
• Checking output for defects, with appropriate and corrective action where necessary.
• Regularly reviewing individual processes and the quality system itself for effectiveness
• facilitating continual improvement

A company or organization that has been independently audited and certified to be in conformance with ISO 9001 may publicly state that it is "ISO 9001 certified" or "ISO 9001 registered". Certification to an ISO 9001 standard does not guarantee any quality of end products and services; rather, it certifies that formalized business processes are being applied.

IQM :

International Quality Management (IQM) is providing ISO Accredited ISO 9001, ISO 14001, OHSAS 18001, HACCP, ISO 22000, ISO 13845, ISO/TS -16949, ISO 29990 & ISO 50001 Certification Services from UASL and ASCB (UK). UASL and ASCB (UK) are the independent and impartial Accreditation’s Board from UK.

Certification procedure :

• In the case of interest for certification of your management system, the procedure is very simple :

  • Complete an Application for Certification form (AfC)

  • On the base of AfC we will process project of the Price Offer (PO)

  • After the acceptation (ratification) of the Price Offer from your side we will prepare a draft of the Contract

  • After the ratification of the Contract by negotiators this Contract comes into force and it becomes legally binding – Contract is signed for 3 years (the validity of an certificate is also 3 years)

  • Within the 3 years’ validity of Contract we conduct 1 certification audit and 2 surveillance audits (vide infra)

• A process of management system certification has these basic phases:

  • Phase of audit planning

  • Assessment of documentation

  • Pre-certification audit (optional)

  • Certification audit

  • Certificate granting and surveillance audits

Phase of audit planning  :

Phase of an audit planning represents planning of an audit. Chief of auditors nominates a lead auditor, an auditor and a specialist from examination scope. Audit team responds to qualified performed audit.

Assessment of management system documentation :

Documentation assessment is performed for the scope of accessory information for planning of a management system certification audit and of monitoring, that there were established basic requirements for proper working of a management system. An auditee is asked to present a quality manual and other reference documentation regarding to standard requirements, according to which the system will have been certified at least 14 days before the audit performance.

Pre-certification audit(optional) :

Pre-audit is performed in the location of a customer with the aim of nonconformities elimination, which can exist in a management system of an auditee. The certification audit is performed in the location of a customer and in the individual working places, which are the object of assessment, according to a customer requests scheduled in the contract. The audit process performance has got these phases :

• Planning (program) – lead auditor determines the timetable with requests for the attendance of individual authorized persons.
• Performance – this stage represents the proper audit performance.
• Completion – team of auditors evaluates the audit performance at the final negotiation with the management representatives of the audited company, the team of auditors assesses dates for elimination of recognized nonconformities.
• Evaluation – the final document of a certification audit is the Certification Audit Report. A Lead auditor prepares a report; he is also responsible for its correctness and completeness. A lead auditor is assessable to add comments of auditors and specialists, who actively took part in an audit, after the personal consultation with them to the report. Certification granting and surveillance audits. If a director of certification body does not find out any significant facts, which should resist to assignments of a lead auditor established in the certification audit report a director of certification body publishes positive consideration with the consideration of a lead auditor and grants a certificate.

The Product Certification Services, provided by us, are widely praised amongst the clients due to high reliability and timeliness. Under Product Certification Services, we provide Services for certain products that have passed performance tests and quality assurance tests requirements stipulated in contracts, regulations, or specifications. Besides, our team of experts caters these Product Certification Services within stipulated time frame as per the requirements of the valued clients.

Product certification or product qualification is the process of verifying that a certain product has passed performance tests and quality assurance tests or qualification requirements stipulated in contracts, regulations, or specifications. For example, it may relate to a building code, nationally accredited test standards, or a set of regulations governing quality and minimum performance requirements. Certifications (and the certificates that document their existence) are often called certs in the everyday jargon of various industries.

ISI Mark (Indian Standards Institution ) :

Formulation of Indian Standards for products and services by bringing together and coordinating various interest groups like manufacturers, consumers, technical experts, testing personnel and others interested. The standards so prepared are known as Indian Standards (IS) and are considered as legal documents. The first Indian Standard formulated was for the National Flag (IS 1). So far BIS has published about 18000 Indian Standards covering various products, codes of practices, terminology, etc for various industrial and economic sectors. The Indian Standards are used not only by the industry but also by the Government, students, consumers and regulatory authorities. The standards are priced publications and are available from all the offices of the Bureau.

CE Marking :

Sai IP Consult Solutions provides support to medical device companies that are seeking CE regulatory approval for their products in Europe. Saiipconsult consultants have a wealth of experience in the preparation of regulatory submissions required to obtain CE marketing clearance and have built strong relationships with the Notified Bodies. Qserve can help you bring your product to the market faster, minimizing the time and costs involved, and maximizing your product revenues.

"CE Mark" means that the product is safe and fit for the purpose for which it was made. Medical Devices Directives (MDD) specify requirements which must be met before permission is granted to apply the CE marking to your medical device and placing it on the market. The Directives which apply to medical devices are :

• Active Implantable Medical Device Directive (90/385/EEC) : This directive covers all medical devices, which rely on a power supply to function and that are left in the human body. These include implantable cardiac pacemakers, implantable nerve stimulators, etc

• Medical Device Directive (93/42/EEC) : The Medical Device Directive covers most other medical devices (active and non-active) and their accessories that are not covered by the first or the third directive. This concerns a large number of products ranging from walking aids to prosthetic heart valves.

• In Vitro Diagnostic Medical Device Directive (98/79/EC) : The In Vitro Diagnostic Medical Device Directive will cover any reagent, reagent product, control material, kit, medical device, instrument, apparatus or system which is intended to be used in-vitro for the examination of substances derived from the human body