黄人导航

Assessments

黄人导航 Compliance Assessments

 

As regulations become more plentiful and stringent, medical device companies face increased issues surrounding compliance. Conducting compliance assessments can help your organization maintain FDA quality standards and enjoy more efficient production. At Regulatory Compliance 黄人导航, we offer an array of assessment services to help you stay within regulatory guidelines and deliver the best products to your end users.

 

Regulatory Compliance 黄人导航 Inc. knows how quality and compliance crises can significantly impact your business鈥攁nd we have the experience to manage them. Our areas of expertise include identifying and assessing any deficiencies to help determine the best approach and solutions.听

 

We’ll work with you to navigate a variety of areas, such as:

 

  • cGMP
  • ISO
  • Quality Infrastructure
  • CAPA
  • Validation
  • Facility and Maintenance
  • PAI

 

FDA 21 CFR 820 Compliance

 

All medical device companies in the U.S. are required to adhere to FDA standards. Specifically, FDA 21 CFR part 820 鈥 also known as the Quality System Regulation 鈥 outlines current good manufacturing practice (cGMP). This regulation sets the standard for the methods and facilities you use to manufacture products and handle design, manufacturing, labeling, packaging, storage and other factors regarding your medical devices.

 

Because the Quality System Regulation outlines such a broad array of requirements, it can be challenging for medical device companies to maintain compliance assessment metrics. Regulatory Compliance 黄人导航 takes the stress out of regulatory compliance with our range of assessment services. You can sit back and focus on your business operations while we identify any challenges in maintaining compliance. We’ll then work with you to thoroughly prepare your metrics and documentation for an FDA inspection.

 

Mergers and Acquisitions / Due Diligence

 

When a life science company considers a merger or acquisition, it is easy to think of the deal’s risk as a potential conflict with the FDA or its equivalent in other countries. The Regulatory Compliance 黄人导航 due diligence team often analyzes a FDA 483, Warning Letter, notified body finding, and/or product recall. But more often, the real reasons a deal doesn’t deliver value are strategic, cultural, or technical. It’s these value-destroying areas that need to be explored during due diligence.

 

Regulatory Compliance 黄人导航 leverages its global experience with acquisitions and divestitures to navigate the gray areas of due diligence and help eliminate uncertainties often inherent in a complex deal. These include:

 

  • Regulatory Due Diligence
  • Quality Due Diligence
  • Facility / Equipment Assessment
  • Personnel Assessment
  • Risk Identification and Mitigation Planning
  • Post-merger Integration

 

Additional services related to assessments include:

  • 21 CFR Part 11 / Annex 11 Assessment
  • 21 CFR Part 820 Assessment
  • ISO 13485 Assessment
  • ISO 9001 Assessment

 

About RCA’s 黄人导航 Consulting Services

 

The regulatory compliance process surrounding the medical device industry involves a strict adherence to pre/post market information throughout a device’s life-cycle. Even a single compliance issue you have can turn into a significant effect on your business. Regulatory Compliance 黄人导航 medical device consultants can help guide you through any stage of this strategic process, with capabilities during product development through the regulatory clearance/approval of your product.

 

Our team of over 500 medical device consultant Experts 鈥 including former FDA officials and regulatory compliance leaders in the field of medical device regulation 鈥 will work with your company to create a quality assurance and regulatory compliance approach tailored to your products and regulatory needs. Regulatory Compliance 黄人导航 works with international Fortune 100 companies, venture capital start ups, and companies of all sizes and shapes. our compliance enforcement solutions for law firms include remediation for warning letters, FDA 483’s, import bans or consent decrees. Very few medical device consulting companies have the same regulatory compliance expertise in a variety of medical fields.

 

Cybersecurity

 

For medical device manufacturers, technology can be a double-edged sword. The innovative technologies that elevate the quality of life for patients can also be used to potentially undermine the organization using the device. The consequences can affect the device itself if Regulatory Compliance 黄人导航 medtech consultants do not implement good IoT cybersecurity and FDA cybersecurity protocols.

 

At Regulatory Compliance 黄人导航, we offer a wide variety of services for medical devices security to help ensure that your product is protected from cyber-attacks. With a well-planned design, along with full visibility of product development and the supply chain, Regulatory Compliance 黄人导航 medical device consultant Experts can help strengthen your device鈥檚 cybersecurity. We partner with medical device companies in each phase of the design cycle, including protecting inputs from threat exposure and hardening outputs for regulatory compliance & FDA submission approval of your medical technology.

 

Regulatory Affairs

 

Regulatory affairs is Regulatory Compliance 黄人导航听backbone, and we handle more submissions in a month than many manufacturers do in a lifetime. Our medical device regulatory consulting Experts have experience working with the FDA, global regulatory bodies and / or agencies, and notified bodies worldwide. Therefore, you can count on us for in-depth and up-to-date insights which increase speed-to-market.

 

As a trusted regulatory affairs consultant, our FDA veterans and industry experts represent Regulatory Compliance 黄人导航 as one of the top medical device consulting firms. We’re here to help you navigate the difficulties associated with new product submissions. Regulatory Compliance 黄人导航 medical device consulting company has expertise in both the approval process and post-approval support.听

 

  • New Product Approval
  • Post-Approval Support
  • Outsourced Staffing
  • EU MDR
  • Combination Products

 

Compliance Assurance

 

Increasingly, life science companies are feeling the pressure of greater scrutiny by regulators, and responding by developing sustainable compliance strategies. Whether it’s preparing for an audit, developing a response to an FDA finding, or remediation to an adverse event, Regulatory Compliance 黄人导航 can help.

 

Our network of over 500 medical device consultants & FDA, MHRA & EMA veterans are industry professionals offers a unique blend of expertise. This allows Regulatory Compliance 黄人导航 to handle both simple and complex regulatory compliance challenges within medical device consulting companies.

 

  • Data Integrity
  • Gap Assessments
  • Internal Audits
  • Employee Training
  • Notified Body Response

 

Quality Assurance

 

Regulatory Compliance 黄人导航 Quality Assurance consulting includes quality system assessments, strategy, implementations, and identification of quality metrics to ensure continuous improvement, aligning with your business needs and goals. Each Regulatory Compliance 黄人导航听medical device consultant is a quality expert with experience spanning major corporations and start-ups. We know firsthand how to achieve, maintain, and improve quality, and we excel in transferring this knowledge to your organization.

 

In the medical devices field, quality assurance (QA) is more than merely ensuring the quality of a finished product. You need the tools to monitor and regulate every process from the design of a new product to continued quality compliance as the device is sent to market. At Regulatory Compliance 黄人导航, we offer you the medical device consultant assistance you need to monitor these processes and ensure quality compliance every step of the way.

 

With more than 20 years experience working with medical device consulting companies, Regulatory Compliance 黄人导航听trusted medical device quality assurance consultant team is fully equipped to handle your unique QA needs.

 

  • ISO13485听
  • 21 CFR 210
  • 21 CFR 211
  • Outsourced Staffing
  • MDSAP
  • Facility Validation
  • Equipment Validation

 

Remediation Services

 

Regulatory Compliance 黄人导航 is widely recognized within medical device consulting companies & the life science industry for remediation services & support. Regulatory Compliance 黄人导航 ability to help companies successfully resolve complex regulatory challenges have a proven track record of success. Our medical device consulting services include significant experience with the development of responses to 483 Observations, Warning Letters, Untitled Letters and Consent Decrees.

 

Our value goes beyond the initial response by helping companies successfully execute their action plans, develop an improved compliance culture tailored to the needs of their business, and ultimately move beyond the regulatory action to emerge as a stronger business. We negotiate difficult demands of remediation with insight and the clear advantage of our medical device consultant expertise and experience that makes partnering with Regulatory Compliance 黄人导航听 a competitive differentiator in the remediation space.

 

  • Quality System
  • Technical File
  • Design History File
  • Data Integrity
  • cGMP听
  • Quality Metrics

 

Strategic Consulting

 

Whether it’s a strategy, a technical plan, or project, Regulatory Compliance 黄人导航medical device consultancy can help ensure a successful project. Regulatory Compliance 黄人导航 medical device strategy consulting can deliver your project on time, on budget, and you’re never embroiled in a costly mistake.

 

Our medical device consultant Experts are industry Experts are here to provide the unique insight you need before an M&A deal, through a staffing crisis and in every area of your product’s development and life cycle. As the trusted medical device manufacturing consultants of thousands of companies around the world, we have the knowledge and expertise needed to deliver exceptional results to your business 鈥 no matter your size or unique needs.

 

  • Manufacturing Optimization
  • Product Lifecycle Management
  • Mergers & Acquisitions (M&A)
  • Due Diligence
  • Device Vigilance
  • Product Complaints
  • Medical Information
  • Risk Management Plan

 

About Regulatory Compliance 黄人导航

 

Regulatory Compliance 黄人导航听(RCA) provides medical device consulting to the following industries for resolution of life science challenges:

 

 

We understand the complexities of running a life science business and possess areas of expertise that include every facet of R&D, operations, regulatory affairs, quality, and manufacturing. We are used to working on the front lines and thriving in the scrutiny of , , and globally-regulated companies.

 

As your partners, we can negotiate the potential minefield of regulatory compliance and regulatory听due diligence with insight, hindsight, and the clear advantage of our unique expertise and experience.

 

  • Founded in 2000
  • Headquartered in Wisconsin (USA)
  • Expertise backed by over 500 industry subject matter experts
  • Acquired by Sotera Health in 2021

 

About Sotera Health

 

The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company鈥檚 unwavering commitment to its mission, Safeguarding Global Health.

 

Sotera Health Company, along with its three best-in-class businesses 鈥 ,听听and听, is a leading global provider of mission-critical end-to-end sterilization solutions and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry-recognized scientific and technological expertise, we help to ensure the safety of over 190 million patients and healthcare practitioners around the world every year.

 

We are a trusted partner to 5,000+ customers in over 50 countries, including 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.

 

Commitment to Quality

 

Our Certificate of Registration demonstrates that our Quality Management System meets the requirements of ISO 9001:2015, an internationally recognized standard of quality.

 

 

To begin the Regulatory Compliance 黄人导航 scoping process today, please enter your information in the blue form below and click the submit button at the bottom of the webpage.听

 

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