Amatya Solutions Private Limited

Amatya Solutions Private Limited Company (A Unit of Amatya Group) Provides 
ISO / IEC 17021 : 2012/15/17 Certification

ISO/IEC 17021 is an international standard that specifies the requirements for organizations providing audit and certification of management systems. The standard outlines the criteria that certification bodies, also known as registrars or conformity assessment bodies, must meet to ensure the impartiality and competence of their certification activities.

The notation "ISO/IEC 17021:2012/15/17" seems to be a combination of the standard's name, its publication year, and potentially some amendments or revisions. Here's a breakdown of the elements:

1. ISO/IEC 17021: This is the core standard that specifies the requirements for certification bodies. It was first published in 2011 (not 2012) as ISO/IEC 17021:2011 and provides a framework for certification of various management systems, including quality management (ISO 9001), environmental management (ISO 14001), and many others.

2. 2012: This might refer to the initial publication year of the standard, which is ISO/IEC 17021:2012.

3. 15/17: It's not clear what "15/17" refers to. It's possible that there may have been amendments or revisions to the standard after its initial publication in 2012. You would need to consult the specific version of the standard or related documentation to understand what these numbers signify.

ISO standards are periodically reviewed and updated to ensure they remain relevant and effective. Therefore, organizations seeking certification should ensure they are compliant with the most recent version of the standard, as it could have evolved since the 2012 edition.

To obtain the most accurate and up-to-date information about ISO/IEC 17021 and its specific requirements, you should refer to the latest version of the standard and any official amendments or revisions issued by ISO (International Organization for Standardization) or IEC (International Electrotechnical Commission) in your region. You can also contact accredited certification bodies for guidance on certification processes based on the most recent standards.

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• Delivery Time: 10 days

Amatya Solutions Private Limited Company (A Unit of Amatya Group) Provides 
Iso 15189 2012 Certification Service

ISO 15189:2012 is an international standard for medical laboratories that specifies the requirements for quality and competence in medical testing and calibration laboratories. Achieving ISO 15189:2012 certification demonstrates that a medical laboratory meets certain standards for quality, safety, and reliability in its testing and calibration processes. This certification is important for healthcare facilities and laboratories to ensure accurate and consistent diagnostic results and patient safety.

Here are some key aspects of ISO 15189:2012 certification services:

1. Documentation and Compliance: ISO 15189 certification services help medical laboratories prepare the necessary documentation, procedures, and quality management systems to comply with the standard's requirements.

2. Assessment and Audit: Certification bodies or auditors assess the laboratory's adherence to ISO 15189:2012 standards through an audit process. This includes a review of documentation, on-site inspections, and interviews with staff.

3. Training and Guidance: ISO 15189 certification services may provide training and guidance to laboratory personnel on how to implement and maintain the necessary quality management systems and processes.

4. Continual Improvement: The ISO 15189 standard emphasizes continual improvement. Certification services may assist labs in identifying areas for improvement and implementing corrective actions.

5. Accreditation: Achieving ISO 15189 certification often leads to accreditation from relevant national or international bodies, which can enhance the laboratory's reputation and credibility.

6. Benefits: ISO 15189 certification demonstrates a laboratory's commitment to quality, accuracy, and patient safety. It can also lead to improved efficiency, reduced errors, and increased confidence among patients and healthcare providers.

7. Regulatory Compliance: In many countries, ISO 15189 certification is a requirement or a strong recommendation for medical laboratories to meet regulatory standards.

Obtaining ISO 15189:2012 certification is a rigorous process, but it can lead to numerous benefits for medical laboratories, healthcare institutions, and ultimately, the patients they serve. Certification services can guide laboratories through the certification process and help them maintain compliance with the standard's requirements. It's important to choose a reputable certification body or service provider to ensure the integrity and credibility of the certification.

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• Delivery Time: 10 days

Overview of FDA Certification. Food and Drug Administration (FDA) established in 1906 is a government agency under the passage of the Federal Food and Drugs Act. It is the oldest comprehensive agency for consumer protection. The FDA Certification is mandatory for placing the products in the USA.

Amatya Solutions Private Limited Company (A Unit of Amatya Group) Provides 
ISO / TS 16949 : 2009 Certification

ISO/TS 16949:2009 is a technical specification for quality management systems in the automotive industry. It was developed by the International Automotive Task Force (IATF) and was based on ISO 9001, the international standard for quality management systems, with additional automotive industry-specific requirements.

Here are some key points about ISO/TS 16949:2009:

1. Purpose: ISO/TS 16949 was created to harmonize quality management system requirements for automotive suppliers worldwide. It is intended to be used by automotive manufacturers and their supply chain partners to ensure quality and safety in the automotive industry.

2. Structure: The structure of ISO/TS 16949 is similar to ISO 9001, with additional automotive-specific requirements. It outlines the core principles of quality management, such as customer focus, process approach, and continuous improvement.

3. Requirements: In addition to the ISO 9001 requirements, ISO/TS 16949:2009 includes specific automotive industry requirements, including product safety, continuous improvement, defect prevention, and a focus on reducing variation and waste in the supply chain.

4. Certification: Organizations can seek ISO/TS 16949:2009 certification by undergoing an audit and assessment by a certification body. Achieving this certification demonstrates a commitment to quality and safety in the automotive industry.

5. Transition to IATF 16949: It's important to note that ISO/TS 16949:2009 was transitioned to a new standard called IATF 16949 in 2016. IATF 16949 incorporates the structure and requirements of ISO 9001:2015. Organizations seeking certification in the automotive industry should consider transitioning to IATF 16949 as ISO/TS 16949:2009 is no longer valid for new certifications.

6. Benefits: Certification to ISO/TS 16949 or IATF 16949 can help automotive suppliers improve their processes, reduce defects, enhance customer satisfaction, and maintain compliance with industry standards. It is often a requirement for doing business with major automotive manufacturers.

Since ISO standards are subject to updates and changes, it's essential to stay current with the latest versions and requirements for quality management systems, especially in highly regulated industries like automotive manufacturing.

Additional Information:

• Delivery Time: 10 days

The Halal certificate is a document that guarantees that products and services aimed at the Muslim population meet the requirements of Islamic law and therefore are suitable for consumption in both Muslim-majority countries and in Western countries where there are significant population group who practice Islam (France, Germany, United Kingdom, Spain). Halal certification is a process which ensures the features and quality of the products according to the rules established by the Islamic Council that allow the use of the mark Halal. It is mainly applied to meat products and other food products such as milk, canned food and additives. Specifically, for meat products Halal certifies that the animals were slaughtered in a single cut, thoroughly bled, and their meat have not been in contact with animals slaughtered otherwise and, especially, with pork. Products that are Halal certified are often marked with a Halal symbol, or simply the letter M (as the letter K is used to identify kosher products for Jewish population).

The word kosher means proper or acceptable, and it has informally entered the English language with that meaning. But kosher laws have their origin in the Bible, and are detailed in the Talmud and the other codes of Jewish traditions. They have been applied through the centuries to ever-changing situations, and these rulings, both ancient and modern, govern OU kosher certification.

You may already be familiar with some of the more well-known requirements for kosher, but you may be surprised at the extent of the regulations with which you are not familiar.

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• Delivery Time: 10 days

Amatya Solutions Private Limited Company (A Unit of Amatya Group) Provides 
Fda Registration

The U.S. Food and Drug Administration (FDA) registration process refers to the regulatory requirements that companies and facilities involved in various aspects of the food, drug, medical device, cosmetic, and dietary supplement industries must adhere to in order to manufacture, distribute, and sell their products in the United States. Here are some key points regarding FDA registration:

1. Types of FDA Registration:

   • Food Facility Registration: Any facility that manufactures, processes, packs, or holds food products for consumption in the United States is required to register with the FDA. This includes manufacturers, importers, warehouses, and other related facilities.
   • Drug Establishment Registration: Manufacturers, repackers, relabelers, or reprocessors of prescription and over-the-counter drugs must register with the FDA.
   • Medical Device Establishment Registration: Companies that manufacture, distribute, or import medical devices into the U.S. need to register their facilities and list their devices with the FDA.
   • Cosmetic Establishment Registration: Cosmetic manufacturers, packers, and distributors are also required to register with the FDA.
   • Dietary Supplement Facility Registration: Facilities involved in the manufacture, packaging, labeling, or holding of dietary supplements must register with the FDA.

2. Registration Process: The specific process for registration can vary based on the type of establishment or product involved. Typically, it involves providing information about the facility, the types of products manufactured or handled, and contact details. Registration is usually done electronically through the FDA's online registration system.

3. Renewal: Most registrations with the FDA need to be renewed on an annual basis.

4. Unique Facility Identifier (UFI): As part of the registration process, each facility is assigned a Unique Facility Identifier (UFI), which is a specific code used to identify and track the facility.

5. Importers and Foreign Facilities: Foreign manufacturers and importers of FDA-regulated products that are sold in the U.S. also need to register their facilities. The FDA requires a U.S. Agent for foreign facilities, who serves as a point of contact between the FDA and the facility.

6. Penalties for Non-Compliance: Failure to register or maintain accurate registration information can result in regulatory action, including fines and even product recalls.

7. Public Access: Some registration information is made available to the public on the FDA's website, including the name and address of the registered facility.

It's important to note that FDA registration is just one part of regulatory compliance. Depending on the type of product and facility, additional requirements for labeling, quality control, good manufacturing practices, and reporting adverse events may apply.

Companies or individuals interested in FDA registration should consult the FDA's official website or seek legal and regulatory advice to ensure full compliance with the applicable regulations. Also, please keep in mind that regulations and requirements may change over time, so it's essential to stay informed about the latest updates from the FDA.

Additional Information:

• Delivery Time: 10 days