ISO Pros in San Francisco, California (CA) is a well-established certification agency founded on decades of business expertise and practice from its senior management. Certifying your organization by yourself can be difficult, costly and time-consuming. Our approach addresses this issue by supplying personnel to insure that the business and services fulfill the growing regulatory requirements easily and without any hassle.
Our goal is to streamline and speed up your certification. Every consumer is exceptional, and ISO Pros is tailoring the service and pricing to their particular needs. If it’s a once-off certification or merely advice on the regulatory road, we are continually questioning the concept of what it entails to be a compliant partner – with a common goal of driving creativity and promoting the emergence of new concepts.
We offer certification services for Quality Management Systems, which allows us to give third party validation to our customers that is globally accredited under the International Accreditation Framework (IAF) umbrella. ISO Pros in San Francisco, California (CA) has built up its credibility with a committed and approachable staff providing competitive certifications programs. ISO Pros interacts regularly with its clients to ensure that any phase of the procedure is as clear as possible, demystifying the qualification process, rendering it a pleasant and satisfying experience.
It is a modern, distinct standard, not an OHSAS 18001-based modification or upgrades historically introduced within organizations. The common essence of the standard rests in its innovation. While OHSAS 18001 obviously has OHS control program specifications, ISO 45001 goes even deeper. The standard does not appear as a requirement collection but centers the OSH culture at the heart of certification. The elements required to be ISO 45001 certified are maintaining secure and stable workplaces, preventing work-related traumas and pathologies, and constantly enhancing OHS efficiency. We may claim that we “do not only” make sure there is a management structure, but it’s also inadequate if OHS isn’t specifically centered in the business culture.
Being certified according to ISO 45001 is not the same as juxtaposing a management system to existing ones. Indeed the standard was developed using the common base of standards ISO 9001 and ISO 14001:2015. Thus, the company should cross-check other aspects of management such as its PDCA strategy, its procedures, or any of its recorded knowledge. OHS is not separate anymore, it is an integral part of the certified organization.
An ISO 9001 certification can make your company a game-changer. This quality certification opens the door for you to be able to sell your product in new markets to new customers — in fact, some customers will only buy from you if you do have it. It’s time to avoid having your rivals grab hold of your business opportunities. According to ISO Survey 2018, there are 878,661 organizations operating over 1 million accredited places with clear ISO 9001 quality management system certificates. If you are not certified, you may lose out.
You will need to find a champion in your company who can sell the idea to your internal leadership team before you can continue the road to ISO 9001 certification. The narrative is all too common. A committed individual has a general understanding of the value of gaining ISO 9001 certification but does not understand the criteria and advantages enough to be willing to successfully market it to other representatives of the organization. And the plan is going to go flat.
It would be a major move in the right direction for the company to have ISO 9001 accreditation just like it has been for many others. Comprehensive knowledge of the criteria and their advantages would place you in a position to be the advocate that your company wants to take that step ahead.
ISO 14001 guarantees the day-to-day implementation of ethical environmental policies through your company. It offers tools and tips for reducing your impact on the environment and improving environmental performance. ISO 14001 lays forth a strategy that should be adopted by a corporation or agency to ensure the execution of an environmentally friendly management system. Any company or association may use it, irrespective of market, operation, or industry.
As with ISO 9001, ISO 13485, and ISO 45001, it is an appropriate management methodology to write structured environmental policies and procedures. Written policies and guidelines are essential to help an organization plan, organize, monitor, enforce, and evolve on an ongoing basis so an agency may further reduce the environmental effect.
An environmental protection scheme according to ISO 14001 will effectively pay for itself both financially and environmentally if properly understood and implemented. We also recognize that services cost money and a wise enterprise will quickly reap the benefits by designing systems to help predict resource use.
As the world becomes more and more environmentally aware (including employees), the smart choice is to implement an ISO 14001-compliant environmental protection system and to enjoy the extra exposure through marketing incentives that come with ISO 14001 certification.
Many countries that develop their medical device regulations based on International Medical Device Regulatory Forum (IMDRF) guidelines rely on QMS compliance with ISO 13485 in their medical device specifications. Each authority made certification with ISO 13485 mandatory as a means of showing conformity with the QMS medical program.
Why would you get an ISO 13485 accreditation?
Whether you’re seeking to operate internationally or expand locally, ISO 13485 Certification can help you improve product performance, raising uncertainty, and raise market prospects. Companies that have this certification provide both customers and regulators with a commitment to protection.
- Improve exposure to more approved customers globally
- Outline how procedures can be checked and enhanced through the company
- Enhance productivity, reduce costs and track supply chain success
- Demonstrate that you are manufacturing better and more effective medical products
Achieving regulatory standards and consumer demands with ISO 13485, which is partially intended to create a management system that facilitates achieving this. Benefits can be reaped by having both 9001 and 13485 approval as 9001 focuses on business problems which are not found in 13485 and support all firms. When the appropriate structure of the management system is in effect it will promote recognition and execution of country-specific specifications for the management system of medical product manufacturers. ISO 13485 is not detailed enough to challenge an individual country’s criteria and will act as a standard management framework for everyone.
AS9100 is the globally recognized standard for the quality control framework applicable to aerospace and defense. The AS9100 standard extends ISO 9001 standards to satisfy the rigorous requirements of defense industries, large aerospace OEMs, as well as producers of general aviation. As an internationally recognized standard, AS9100 guarantees entities across the globe are consistent with rigorous standards of quality, safety, and reliability.
This AS9100 certification represents your company’s ongoing effort to follow the specifications for aerospace components. Your business has continuously exceeded its consumers’ needs and getting certified will help you to continue to do so, with a new acknowledgment of our commitment to unrelenting excellence. It will also strengthen the strategic position across many of your departments through rigorously standardizing performance, reliability, and security procedures.
The AS9100 certification will be the standard against which all aerospace suppliers have been measured and it reflects the ongoing production efforts and commitment of your workers in supplying the finest performing products. The introduction of your AS9100 certification complements will illustrate your focus for supporting the challenges and demands of the transport, aerospace, medical industries, and security industries.
IATF 16949:2016 is a formal standard for automotive quality control systems established by the International Automotive Task Force (IATF), which attempts to harmonize the different supply chain measurement and evaluation processes worldwide. IATF 16949:2016 framework incorporates current automobile customer-specific requirements and is a supplement to ISO 9000/9001:2015 guidelines for car production and associated service system organizations.
Implementing IATF 16949:2016 will assist any member of your team who is interested in planning, conducting, and executing the QMS audit activities of your organization and implementing its environmental policies.
Since ISO 9000 was launched, as many industries have done, the automotive business couldn’t help but feel extremely generalized. Many countries had since developed their very own automotive-based variants. Of course, the standard appeared to be different from one nation to another. So the International Automotive Task Force (IATF) has since been established to develop the requirements for international quality standards specifically for the automotive industry. There is now a partnership between the IATF and International Organization for Standardization with the participation of large European and North American automobile designers, dealers and car exchange partners
This official certification was developed to serve as a quality management system for designing and developing, manufacturing, installing, and servicing automobile-related products and, more importantly, harmonizing standards for automakers around the world.
The most current consistency standard for the automobile industry is IATF 16949 today. This technological standard is incredibly stringent, ensuring machine shops are able to increase their work efficiency and automate their processes. When the machine shop wants to receive the certification, there are a variety of steps to be taken to prepare for an audit, including conducting a study of the gap analysis as well as educating the organization.
The Cybersecurity Maturity Model Certificate is a special qualification designed for contractors of the Defense Department (DoD). It defines data privacy requirements for entities that operate for, or are part of a supply chain for the DoD, Federal Contract Details (FCI) and Controlled User Information. The certification is far simpler than previous data protection systems, which allowed the contracting authority to apply with an enforcement plan for the network and devise an action plan and objectives to meet with the DFRAS.
Certification information for CMMC
The CMMC certification comprises 5 competence levels, from basic level 1 hygiene tests to the latest level 5 advanced controls. The higher the degree a company is certified to, the more stable it is. Having a certification level which is higher means the company can perform additional jobs and is therefore available for further contracts.
How DoD contractors are impacted by certification with CMMC
Having CMMC can help DoD contractors ensure the appropriate cybersecurity standards are met for their operations. An organization that wants to have a contractual agreement with DoD or that operates on a department project as a subcontractor needs certification. For companies, the benefit of CMMC is the opportunity to bid for work, as they are more likely to receive projects because they are accredited to a high CMMC standard.
Another advantage of having CMMC certification is eliminating ambiguity in the specific DoD sector with respect to security compliance. Its credential verifies the conformity of an organization with cybersecurity policies and practices, including their attempts to secure the equipment including networks established by the defense industrial base (DIB)
How ISO Pros in San Francisco, California (CA) can help
At ISO Pros we are helping DoD contractors reach an appropriate safety level by evaluating all software systems and networks. Our team will periodically support DoD contractors in their CMMC’s requirement and evaluation phases, and the correct CMMC standard will be assessed on the basis of ISO Pros auditors’ assessment report.
CMMI approval can improve a company ‘s credibility by showing customers that its products and services follow the criteria. In some cases, or in some industries, certification is required or legally mandated. The certification process involves applying the CMMI qualification criteria and then conducting a functioning registrar’s examination to ensure the company meets certain specifications.
If a company doesn’t have insight into their internal management processes, how else would an organization realize how good they’re doing before it is too late. CMMI carries out mechanisms that look at all kinds of innovations and best practices. It is a starting point, not a final goal. CMMI can not tell a person what is, or what isn’t, important to them. Nonetheless, CMMI can provide a roadmap for a business to achieve its goals of success.
CMMI is merely a concept, however, it is not reality. Unlike every other concept, CMMI reflects one definition of truth and like most models, it is rather idealistic and unrealistic, at least in certain respects. When it is known as “only” a model, there is a much greater chance that individuals using CMMI can implement something of permanent importance. What is missing from CMMI as a model is a context. In accordance with the company context, CMMI may be implemented to build a process management approach that matches the context of each particular enterprise.
To bring it all together, CMMI is a blueprint for developing process enhancement frameworks from which (astute) companies derive and develop process enhancement solutions that suit their particular context to help increase their organizational efficiency.