We provide certified licensing, instruction, and support resources to assist you in optimizing processes, results, and resources. We provided many certificates to consumers in many states.
We support organizations of all sizes to do their best in handling efficiency, climate, energy, productivity, health, and safety. In fact, we help maintain that these changes happen year in year out. Your organization will collaborate together with our experts who will play a vital part in developing such management systems. They have the luxury of partnering with numerous organizations, from small companies, foundations, government agencies, and world-renowned brands such as NASA.
- Our dedication to achieving the highest customer satisfaction quality is embodied in our Consumer Charter:
- We will listen to you and make the very best effort to have the best answers
- We pledge professional guidance, technological know-how, and highly qualified people to help you
- We’ll offer services customized to suit your needs as your company expands
- We’ll offer competent and prompt support
- We will be also polite, courteous, and supportive.
The philosophy of ISO Pros in San Jose, California (CA)
Every company should do better, in a reliable, continuous and sustainable manner. That’s all we believe in at ISO Pros and working to do it, is what we are here for. Our services of evaluation, qualification and training allow businesses to adopt reform, develop management processes and prepare for potential growth.
ISO 45001 is the worldwide universal standard for workplace health and safety, provided to shield workers and visitors from injuries and diseases linked to employment. ISO 45001 certification has been established to eliminate any variables which may inflict irreparable damage to staff and companies. Its requirements are the culmination of tremendous work from a group of health and safety policy professionals who have closely looked at a range of other program implementation methods — including ISO 9001 and ISO 14001. Furthermore, ISO 45001 was planned to take into account certain current workplace health and safety requirements such as OHSAS 18001 — as well as labor regulations, norms, and protection protocols of the ILO.
Specially targeted for senior managers, ISO 45001 has the primary aim of helping companies provide their staff and anyone else who enters the workplace with a safe and efficient working atmosphere. This goal can be done by monitoring variables that might theoretically contribute to injuries, disease, and even death in serious circumstances. As a consequence, ISO 45001 is concerned with eliminating all causes that are detrimental to the physical and/or emotional well-being of the staff or present a risk.
Sadly, thousands of employees are losing their lives every day as a consequence of preventable cases of hazardous circumstances at work. In addition, more than 2.7 million fatalities occur worldwide due to workplace injuries according to the ISO and International Labor Organization — or ILO. And on top of this, there are 374 million non-fatal accidents per year, culminating in 4 or more days of job absences.
The advantages of introducing quality control programs include improved operating efficiency; an ability to objectively analyze how workers perform their job and communicate with each other; setting up suitable procedures for potential operations; clearer recording of approaches and responsibilities; process consistency; enhanced knowledge of quality among workers; cost savings from less waste.
The Advantages of ISO 9001
Implementing a quality control program can inspire workers by identifying the main tasks and duties they have. Price reductions will be achieved by increasing performance and quality because weaknesses in the product or service would be stressed. Upgrades may be created from this, resulting in less duplication, inadequate or rejected jobs, and fewer grievances. Customers can note that requests are being met reliably, on schedule, and according to the appropriate requirements. It will free up the market to further possibilities.
Audits according to ISO 9001
When the ISO 9001 criteria are fulfilled, it’s time for an external audit. A third party, certified classification body (CB), such as ISO Pros, will conduct this. The appointed CB should study the manuals and procedures for consistency. This method includes looking at the quality assurance by the organization and ascertaining if the goals established by the management system are tangible and achievable. It is accompanied by a complete on-site evaluation at a later date to ensure all job activities meet the protocols and specified targets and that correct documents are kept.
Implementation of an environmental management system ISO 14001 offers a clear starting point for different job practices and new contracts in numerous economic divisions. What’s more, an environment management system conforming to ISO 14001 would allow you to:
- Reduce the Company’s negative environmental impacts;
- Cost savings by energy recycling, improved usage of raw materials, reduced waste and, finally, improved cost of waste management;
- Command of emergency incidents utilizing the technique for mitigation and remedial response plans;
- Speeding up the process of government acceptance, diminishing control over policy;
- Boost competitiveness, both at home and abroad;
- Strengthen your image and prestige with employers, partners, and supporters;
- Obtain regulatory protections by implementing applicable environmental legislation.
The certification is meant to confirm an entity’s capacity to manage the practices and procedures related to environmental concerns. This standard extends to all organizations, regardless of their context.
ISO 13485 lays out criteria for a QMS in which an organization has to demonstrate the capacity to deliver medical devices and related services that consistently meet consumer demands and legislative requirements unique to medical devices and related services.
The primary purpose of ISO 13485:2016 is to facilitate harmonized regulatory requirements for quality assurance systems in medical devices. As a consequence, it includes certain basic requirements for medical devices and excludes any of the ISO 9001 guidelines that are not suitable as implementation specifications.
Your products and capabilities will include:
High-level consultation, where we ask the following questions:
- What is the structure of QMS?
- What methods and procedures do you need to use to get the system to work?
- Do you feel comfortable the QMS will survive a regulatory audit?
ISO 13485 QMS models.
Our consultants have developed robust and detailed QMS frameworks through the years of working for numerous organizations. Based on our latest findings and any regulatory changes these models are continuously being established and updated.
Experienced qualified paper writers
Our paper writers are experts in plain English and have a wide selection of QMS documents on which they can call upon.
AS9100D is an internationally recognized certificate in quality and safety that demonstrates a company’s compliance with the highest standards in aerospace, aviation, and defense industries. Regulation and/or compliance of AS9100 is a common condition for doing business for many businesses in those aerospace and defense industries.
However, AS9100 combines all the characteristics of the ISO 9001 standard with a multitude of different standards to satisfy the challenging specifications of clients in the fields of aerospace, defense, and aviation, concentrating heavily on end-to-end manufacturing processes, risk management, and efficiency growth.
AS9100D is the current iteration of the AS9100 specification, with several new sub-clauses that put greater focus on consistent security and falsified part avoidance. It also complies with ISO 9001:2015 to get the design of this simple system into order.
This certification lets you work on both aerospace and military-specific goods and reinforces your position as a high-quality, trustworthy manufacturer within these sectors. Your processes and products will be of the highest standard and have full approval.
These requirements are usually incorporated in a robust aerospace design system. The industry experts who established the standard agree that certain elements, including high-quality products, procedures, and facilities, are necessary to sustain its safety. While the specification determines market criteria for a QMS, the system managers are also accountable for the implementation process.
The main changes for IATF 16949 includes::
Risk and safety management
The latest IATF 16949 lays out clear risk control criteria. We seek to recognize and minimize danger in order to reduce weaknesses in the implementation of innovative projects as well as enhancing the execution of scheduled activities. The updated standard also allows companies to provide systems that can guarantee patient protection over the whole product lifecycle.
Such best practices have been targeted at promoting a more safe and efficient sector.
Specific customer specifications
This framework explicitly separates consumer specifications from Consumer Specific Specifications (CSR) to prevent confusion and defines the protocols for resolving them.
The traceability of goods
IATF 16949 requires the enhancement of product traceability standards to facilitate legislative reforms specific to this industry.
Required specifications for products that have embedded software
With advancements in electronics, technology and software are already integrated into cars, this is something which hasn’t existed before; therefore, the regulation already specifically discusses certain devices and information systems which are installed in automobiles.
The Under-Secretary of Defense for Acquisition & Sustainment has announced a new cybersecurity framework that a third party professional assessor (C3PAO) would allow all Department of Defense companies to agree with and be accredited. The standard is expected to come into force in November 2020.
How can ISO Pros in San Jose, California (CA) assist you?
Gap analysis/ Readiness assessment
Pursuant to the CMMC system, we perform a 3-6 week evaluation of your company. You get a report card that defines each protection control you require and an enforcement decision for each regulation. They include actionable guidelines for remediation of places of non-compliance that can quickly be turned into a POA&M.
Our team contributes its expertise to help resolve your enforcement problems, supplementing your own staff if appropriate. We are your outsourced one-stop-shop, compliant with CMMC, keeping you efficient when laws change, now and in the future.
Our devoted CMMC Compliance Managers meet the team to ensure that the security program needed to pass the certification is implemented. Includes written documentation & procedures, ongoing monitoring, independent analysis & control functions, and CMMC’s required cybersecurity training program.
Security and Governance
Everything from our Governance System, and our controlled security service approved by FedRAMP. Includes all licenses for the network hardware and security software, configured securely to CMMC requirements, managed and monitored by us.
Increasingly company practices with a view to improving efficiency and rising savings is a problem confronting multiple businesses worldwide today. This is especially true of governmental and commercial organizations that are attempting to identify process enhancements for combined product and service creation, information engineering, and system design.
Capability Maturity Model ® Implementation (CMMI) is an approach to process management that incorporates the basic elements of successful systems that eventually increase their efficiency. This may be used to direct the development of operations within a project, group, or organization.
ISO Pros in San Jose, California (CA) has your CMMI solution
ISO Pros provides the most sophisticated and robust risk monitoring software system that follows the rigorous criteria of the CMMI methodology. Our expert support allows companies to adopt the strategy, thus lowering regulatory expenses, optimizing performance, increasing efficiency, and reducing harm.
The tools from ISO Pros enable companies to quickly implement CMMI, provide services to handle operations, assessments, non-conformances, quality KPIs, quality documents and reports, improve operational performance, minimize rework and waste. Organizations and administrators will collaborate and be informed on the performance improvement programs through electronic networking tools, including additional participants, departments, divisions, and business units in a structured and cohesive strategy, transforming quality recommendations into behavior.