We are ISO certification consultancy service provider in Delhi NCR & other cities of India.
We consulting for ISO 9001, ISO 14001 Environmental Management System, OHSAS 18001, ISO 45001, ISO 22000 (Food Safety Management System), ISO 20000 ITSMS, ISO 27001 ISMS, ISO 26000 CSR, FSSC 22000, HACCP, BRC & BRC IOP, ISO 22716 Cosmetic GMP-Goods Manufacturing Practice, GDP certification, ISO 26000, Social compliance audit, Factory audit, SEDEX registration, SMETA 2-Pillar & 4-Pillar audit, BSCI Audit, factory quality audit, Walmart FCCA audit, C-TPAT certification, SA-8000 certification, Global Organic Textile Standard (GOTS), OEKO-TEX certification, ISO 13485 for medical Devices, TS/IATF 16949, CE Marking, Forest Stewardship Council (FSC) certification etc.
4B Solutions is actively engaged in offering its services in diverse business areas of ISO consultancy, Software and HR Solutions.
GFSI, BRC, FSSC 22000 certification in Baddi, Kashipur, Haridwar, Delhi, Noida, Gurgaon, Pune, Haridwar, kanpur, Allahabad, Mathura, Bikaner, Jaipur, Kundli, Rohtak.
Social compliance audit (SEDEX, BSCI, SA-8000, C-TPAT, OEKO-TEX, GOTS, ISO 26000 CSR) consultants in Delhi, Noida, Agra, Gurgaon,Kanpur, Jaipur, Jodhpur, Surat, Pune, Mumbai, Moradabad, Mathura, Okhla, Baddi, Solan, Kundli, Jalandhar, Ludhiana, Karnal, Panipat, RIICO Industrial area.
Haccp certification in India.
ISO 22000 certification in India.
Brc certification in India.
Fssc 22000 certification in India.
ISO 9001 certification in India.
ISO 13485 certification in India.
ISO 14001 certification in india.
Ohsas 18001 certification in Bhopal, Jabalpur, Satna, Rewa,Delhi.
Ce marking certification in India.
ISO 26000 CSR certification in India.
False2018-11-24T12:38:29We provide NABCB ISO Certification Consultancy Services for ISO 9001, ISO 14001, ISO 22000, ISO 45001 that give you in depth knowledge about various benefits i.e., it improves quality and productivity, creates awareness among staff about the quality of products, reduces wastage, improves internal communication etc.
We offer to our clients,our expertise and assistance for getting their organizations ISO certified. The certification is based on good system & processes practiced by the concerned party and quality of it's products or services. Our team of experts has extensive experience in designing and implementing corrective and preventive action systems that prevents problems from recurring in future.
Benefits from ISO:
Better management of core business processes
Increased awareness of quality among staff.
Improved productivity and quality.
Improved internal communications.
Reduced wastage and cost per unit/service.
Some of the facilities offered by us :
Writing ISO quality manual,procedures,formats/records.
Establishing company's quality policy & measurable quality objectives.
Creating efficient system for controlling distribution and re-issue of
True2018-11-01T15:46:57A social audit is a way of measuring, understanding, reporting and ultimately improving an organization’s social and ethical performance. A social audit helps to narrow gaps between vision/goal and reality, between efficiency and effectiveness. It is a technique to understand, measure, verify, report on and to improve the social performance of the organization.
Social auditing creates an impact upon governance. It values the voice of stakeholders, including marginalized/poor groups whose voices are rarely heard. Social auditing is taken up for the purpose of enhancing local governance, particularly for strengthening accountability and transparency in local bodies.
The key difference between development and social audit is that a social audit focuses on the neglected issue of social impacts, while a development audit has a broader focus including environment and economic issues, such as the efficiency of a project or programme.
Objectives of social audit
Assessing the physical and financial gaps between needs and resources available for local development.
Creating awareness among beneficiaries and providers of local social and productive services.
Increasing efficacy and effectiveness of local development programmes.
Scrutiny of various policy decisions, keeping in view stakeholder interests and priorities, particularly of rural poor.
Estimation of the opportunity cost for stakeholders of not getting timely access to public services.
Advantages of social audit
(a) Trains the community on participatory local planning.
(b) Encourages local democracy.
(c) Encourages community participation.
(d) Benefits disadvantaged groups.
(e) Promotes collective decision making and sharing responsibilities.
(f) Develops human resources and social capital60000
True2018-09-24T13:39:58What is ISO 45001?
ISO 45001 was published on March 12, 2018 and is the new international standard for occupational health and safety (OH&S) management
ISO 45001 specifies requirements for an occupational health and safety (OH&S) management system and gives guidance for its use to enable organizations to provide safe and healthy workplaces by preventing work-related injuries, illnesses, and fatalities and by proactively improving OH&S performance
ISO 45001 is applicable to any organization worldwide regardless of its size, type, or nature
ISO 45001 replaces OHSAS 18001, the world’s former reference for OH&S management (organizations currently certified under OHSAS 18001 will have until March 12,2021 to migrate to ISO 45001)
False2018-07-18T16:29:56A CE mark is a symbol that must be affixed to many products before they can be sold on the European market. The mark indicates that a product …
Fulfills the requirements of relevant European product directives.
Meets all the requirements of the relevant recognized European harmonized
performance and safety standards.
Is fit for its purpose and will not endanger lives or property.
The presence of CE marking further indicates that appropriate technical documentation supporting the use of the mark is available and can be provided by the manufacturer, importer, or person responsible for placing the product on the EU market upon request.0
True2018-07-12T03:30:40The BRC Global Standard for Storage and Distribution is designed for companies that store and/or distribute food, consumer products and packaging material.
This Standard is designed to promote best practice and facilitate a process of continuous improvement through well designed risk-based product safety management systems. The goal of the Standard is to ensure that the quality and safety of products during their storage and distribution is maintained. Certification to this Standard is an indication to buyers and consumers that the supplier has met rigorous international benchmarks in best practice, risk assessment and quality system.
Issue 3 of this Standard has been developed by a multi-stakeholder group including retailers, food service companies, industry trade associations, independent experts and certification bodies, and builds upon the experience from the previous issue.
In the Introduction to the Standard, the BRC identifies the following benefits of certification to the Standard:
It is an internationally recognized Standard which provides a report and certification that can be accepted by buyers in place of their own second-party audits – reducing the time and cost involved with multiple, second-party audits.
The comprehensive scope, covering areas of quality, hygiene and product safety, provides a benchmark to best practice in storage and distribution industries.
When effectively adopted, it can reduce damage and waste, thereby reducing cost.
Greater credibility and recognition are achieved with certification.
Certificated sites may appear in the BRC directory allowing recognition of their achievement and the use of a BRC logo for marketing purposes.
Certification addresses the due diligence requirements of both the certificated company and the buyer.
Ongoing surveillance and follow-up corrective actions after an audit help to ensure that a self-improving quality, hygiene and product safety system is established.
True2018-05-08T13:50:53ISO/TS 16949 is now IATF 16949.
In October 2016 the latest revision of the most popular Automotive Quality Management Standard was Published, and this became IATF 16949.
IATF 16949 is an internationally recognised standard for quality in the automotive industry developed by the International Automotive Task Force (IATF), which is made up of the world’s leading automotive manufacturers.
Major car manufacturers recognise the value of IATF 16949 in their supply chain, and achieving this standard can benefit your business during the tendering process.
However, IATF 16949:2016 is not intended to be a stand-alone Quality Management System. Instead the supplementary requirements should be incorporated into an ISO 9001 Management System.
The certification lasts for 3 years, during this time a series of internal and external audits will be conducted to ensure the management system is meeting its objectives.
We can help you achieve certification and maintain the IATF 16949 Management system through internal audits and improvement advice.1500000
True2018-05-02T15:50:53Organisations seeking to approach CSR in a structured and reliable manner can benefit greatly from the ISO 26000 guidelines for social responsibility.
4B Solutions, with a tailor-made assessment tool, can measure a programme’s performance and identify improvements and risks linked to an organisation’s business strategy.
Social responsibility has become a major topic in recent years, arising from mounting pressure from the public sphere and stakeholders at large. The need for credible business practices that demonstrate social responsibility, performance, as well as achieving outstanding results, is clear.
To respond to these issues, the International Organization for Standardization launched the first voluntary guidance on Corporate Social Responsibility.
The aim is to actively promote credible reporting, company accountability and improve market performance.
The core subjects identified in ISO 26000 are related to different areas and are closely tied to the governance strategy of the organisation:
Community and Development40000
True2018-04-27T15:18:474B SOLUTIONS provides a rational and cost effective solution to avoid social compliance issues, our Social Compliance Audit service. Employing a multi pronged approach using proven investigative techniques to gather and corroborate factory information, our native language auditors conduct comprehensive confidential staff interviews, records analysis, and assess all factory operations based on globally recognized compliance benchmarks.
As companies expand their sourcing efforts in developing countries, it becomes increasingly important to scrutinize supplier workplace conditions. The conditions under which products are manufactured have become an element of quality and an important part of the business value proposition. Lacking a process for managing risks related to social compliance may have a direct impact on a company’s bottom line. This is especially true where image and brand are critical assets.
4B SOLUTIONS has the capability and resources to support your effort to develop an effective social compliance program, as well as conduct audits of compliance-related processes and controls for you.
Our Social Compaince Audit includes evaluations of your supplier’s compliance with:
• Child labor laws
• Forced labor laws
• Discrimination laws
• Minimum wage laws
• Worker living standards
• Working hours
• Overtime wages
• Social benefits
• Safety and health
• Protection of the environment
Social compliance audit-SA-8000, Sedex/SMETA/ETI. COC. BSCI, Factory Audits & Supplier Audits for Manufacturer.60000
True2018-04-21T13:38:01The Customs-Trade Partnership Against Terrorism (C-TPAT) program is the partnership between the U.S. Customs and Border Protection (CBP) and the supply chain community to focus on protecting the United States against acts of terrorism by improving security while speeding the flow of compliant cargo and conveyances.
5 Step Risk assessment, threat assessment, systems, third party audit, documentation and corrective action plans are all covered including how to produce a supply chain flow chart for each supply chain.
To establish policies enhancing their own security practices and those of business partners involved in the supply chain, based on the following C-TPAT security criteria:
Business Partners Requirements
Physical Access Controls
Security Training & Threat Awareness
Information Technology Security
Once these policies are given an effect, imports by these businesses would be given a “Fast Lane” by the US Customs. 90000
True2017-11-18T07:33:23PS 9000 adopts a risk assessment approach to the identification and implementation of preventive action and uses case studies to illustrate areas of GMP risk.
PS 9000 is a standard relevant to all parts of the pharmaceutical industry supply chain, allowing shared knowledge, practices and implementation to manage risks and safeguard the well being of people and business.
Whether a contractual need or simply looking to reduce overall risk to your organisation and products, there are a number of key benefits to implementing a certificated PS 9000 system.
Quality Controls - Clear implementation of practices across production process including electronic interfaces to assure quality products, fit for purpose and minimising counterfeit medicines
Personnel/Communication - More clearly understand roles and responsibilities in terms of producing quality products
GMP - Incorporation of specific Good Manufacturing Practice requirements which assure material are appropriate quality and correct procedures are followed in terms of checking, traceability, contamination and hygiene controls
Risks - Structured approach to risk management and key focus on risk areas associated with packaging operations, with effective controls and activities detailed, which ultimately helps to reduce potential product and business issues
Compliance - Used in support of regulatory compliance and identification of appropriate legislation
Harmonisation - Helps integration of Regulatory, Quality and GMP requirements
Commitment - Organisations need to show their compliance with all relevant statutory and regulatory pharmaceutical packaging safety and GMP requirements in addition to their own policies.
True2017-11-16T09:21:00ISO 9001 certification is suitable for all sizes and types of organizations and is well established around the world as an invaluable Quality Management System standard. It is suitable for organizations in all industry sectors and will help your organization to improve management processes to compete locally and or globally.
Benefits of ISO 9001:2015 Standard:
Sets out areas of responsibility across the organization
Communicates a positive message to staff and customers
Identifies and encourages more efficient and time saving processes
Reduces your costs
Reduce your Internal Rejection
Provides continuous assessment and improvement
Benefits of customers:
Improved quality and service
Delivery on time
Fewer returned products and complaints
Independent audit demonstrates commitment to quality
ISO Certification Process:
Approval of Application form
Stage 1 Audit
Stage 2 Audit
True2017-10-14T08:51:31SOC 1, 2 and 3 are audit reports awarded to service providers demonstrating a defined level of security controls. SOC 1, 2 and 3 do not provide certification to any international standard.
They are audits developed by the American Institute of Certified Public Accountants (AICPA) primarily to meet the needs of American companies.
They have not been through the rigorous international review process common to international standards, and as such may disregard regional issues that tend not to exist in America.
SOC 1, 2 and 3 audits can only be conducted by a Certified Public Accountant (CPA) registered with the American Institute of Certified Public Accountants.
SOC 1 is an audit report on controls related to the protection of financial statements. This report is only likely to be relevant to those service providers that offer financial reporting services.
SOC 1 audits are performed against an American standard called SSAE 16.
SOC 2 is an audit report on controls related to one or more of the following areas: security, availability, processing integrity, confidentiality and privacy. The scope of the report varies depending on which of these attributes the service provider decides to include.
SOC 2 audits are performed against American standards known as the Trust Services and AT 101.
SOC 1 and SOC 2 reports can be either Type 1 or Type 2. A Type 1 report is restricted to an assessment of how the security controls are designed. It does not include an assessment of how effectively the controls are operating. A Type 2 report includes an assessment of the design and operating effectiveness of the security controls.
SOC 2 reports are generally not provided to service providers’ clients because they may contain sensitive information about security controls. Instead, a service provider can obtain a higher level compliance report called SOC 3, which does not contain sensitive information. The assessment for SOC 2 and SOC 3 is the same, but the report is different. The SOC 3 report can be provided to clients to demonstrate compliance without disclosing any sensitive information. SOC 3 reports must be performed as a Type 2 assessment.
True2017-07-01T17:44:56The Global Organic Textile Standard (GOTS) is recognised as the world's leading processing standard for textiles (clothing, home textiles, & personal care products) made from certified organically produced raw materials.
It includes strict environmental & social criteria for operations along the entire textile supply chain. GOTS is globally recognised, & the numbers are growing – in 2014 more than 3600 facilities worldwide were certified to GOTS.150000
True2017-05-20T17:38:51Good Distribution Practice (GDP) refers to the regulatory guidelines governing the wholesale distribution of medicinal products to ensure their quality and integrity is maintained throughout the supply chain from the manufacturer to the end user.
Good Distribution Practice extends beyond the distribution of the finished product and includes the sourcing, storage and transportation and other ingredients prior to manufacturing.
Failure to adhere to the guidelines at any point within the supply chain, including all intermediate points of storage and transport, can have a serious impact on the quality of the product.
Distributors and Importers require Good Distribution Practice for Medical Devices (GDPMD) certification.
Good distribution practice (GDP) deals with the guidelines for the proper distribution of medicinal products for human use.
GDP is a quality warranty system, which includes requirements for purchase, receiving, storage and export of drugs intended for human consumption.
The GDP requirements consist of 6 parts:
2. Organization and GDP Regulatory Compliance System
3. Establishment Responsibilities
4. Resource Management
5. Supply Chain and Device Specific
6. Surveillance and Vigilance
True2017-04-04T13:21:50BIFMA is the Business and Institutional Furniture Manufacturers Association.
BIFMA is satisfied to declare that the level sustainability certification program for furniture has exceeded the manufacturer mark on the quickly growing list of companies who produce level certified products.
Points earned under each of these categories determine the level of certification earned:
*.Level 1. The first tier of certified presentation
*.Level 2. Additional milestones of presentation
*.Level 3. The highest level of presentation
True2017-04-04T13:15:24ISO 28000:2007 identifies the needs for a security management system, including those aspects dangerous to security assurance of the provide chain. Security management is linked to many other aspects of business management. Aspects include all activities controlled or prejudiced by organizations that impact on supply chain security.
ISO 28000:2007 is appropriate for all sizes and types of organizations that are involved in the production of goods, manufacturing, services, storage or transportation at any stage of the products, enlargement or movement in the supply chain.150000
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