Quality Assurance Service Companies-2021
Pharma Tech Outlook
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Top 10 Quality Assurance Service Companies - 2021

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Quality has always been the cornerstone of the safe and effective development of drug products. With quality assurance being a critical element to pharmaceutical manufacturing, pharmaceutical companies are set to improve further by leveraging rapidly advanced technologies such as AI, blockchain, IoT, data analytics, and much more.

Notably, with an AI tracking system, pharmacists are able to verify the authenticity of the information. And also, by leveraging IoT-enabled devices, pharmacists can track patient health data like heart rate, blood pressure, and more. Such real-time information derived from health data helps pharma companies researchers to make informed decisions throughout drug administration that in turn increase efficiency and reliability in quality control. And once the product is on the shelf at the pharmacy, the pharmacists and the patients can use the same software to verify the product’s origin. Additionally, machine learning algorithms can automatically adjust manufacturing lines depending on demand and also serve as a proactive source of any anticipated roadblocks. This realtime responsive decision-making is driving quality assurance improvements and is fast becoming crucial to ensure operational efficiency for manufacturers.

At this juncture, there is a variety of quality assurance service companies available in the market that cater to the different needs of enterprises and organizations. To help them choose the company that best fits their requirement, Pharma Tech Outlook has compiled a list of the top 10 quality assurance service companies. The enlisted companies are the frontrunners in the market that provide a wide span of features. Besides, the magazine also comprises insights from thought leaders in the sector on the industry trends, best practices, recent innovations, and their advice for aspiring CXOs.

We present to you Pharma Tech Outlook’s “Top 10 Quality Assurance Service Companies – 2021.”

    Quality Assurance Service Companies

    Compliance Insight's experts will help evaluate and remediate clients' compliance issues, address problem areas, and develop the type of Quality Culture that will help minimize errors and maximize production. Compliance Insight offers a partnership with client rather than just delivering a service by focusing on a three-step program for developing GMP habits. Step one is the most important—and one that most people miss—is to understand the “why” of GMPs. To develop an understanding of the purpose and personal meaning of GMPs or quality is essential. After that, we then pick up on next two steps: the how and what of GMPs. ... read full profile
    Contract Pharmacal Corp. (CPC) develops, manufactures and packages solid dose drugs and dietary supplements. CPC employs more than a thousand highly skilled professionals in its Hauppauge, NY facilities totaling 500,000 square feet and to date has commercialized over 5,000 products. The company develops approximately 100 new products per year, and has capacity to support manufacturing 15 billion tablets and capsules annually. CPC's customers rank among the world's top pharmaceutical companies, retailers and wholesalers. More than 60 customers around the globe rely on CPC from the early stages of product innovation and development to commercial manufacturing and packaging. ... read full profile
    Cromos Pharma is a US-based, international CRO that offers services regarding clinical trials in all clinical phases and therapeutic areas. The company offers fully integrated CRO services, including clinical development strategies, analysis of local standards of care, regulatory compliances, pharmacovigilance and safety support, as well as quality assurance and biostatistics services. Cromos Pharma’s unique “No Patients - No Payment” risk-sharing initiative is unheard of in the industry and consolidates its commitment to provide the highest quality of services to its clients. Founded in 2004 by Dr. Vlad Bogin, the company has a strong presence in Central and Eastern Europe and in the US ... read full profile
    The company brings executive-level quality-focused leadership to FDA regulated business leaders reducing the full-time headcount cost of an executive-level GxP professional ... read full profile
    With TRI’s technical expertise, management experience, and operational framework, clinical trial sponsors can develop and review their own quality management programs to facilitate effective clinical research implementation, verify data accuracy, and promote a constant state of readiness for an external audit or regulatory inspection. TRI’s program activities include Quality Management Systems (QMS) Development; Auditing Services; Compliance Services, such as for 21 Code of Federal Regulation (CFR) Part 11 and 45 CFR 46, and International Organization for Standardization (ISO) certification readiness; Support Services for regulatory agency inspection readiness and enforcement action; and Validation Services ... read full profile
    Altus Quality
    Altus Quality is a top-tier consulting group headquartered in the dynamic commonwealth of Massachusetts, and just a few miles outside of the biotech hub of Cambridge. Altus provides Quality and Compliance advisory services to the Clinical and Life Science sector. Our Passionate Professionals provide GxP Auditing, Process Development/Technical Writing and QMS Support. We believe in the synergy of people and processes. When properly combined, efficiency is lean and value is invaluable. Altus Quality is proudly certified as a MWBE organization.
    GxP Central
    GxP Central, with headquarters in Las Vegas, Nevada, is a subsidiary of Quality Resource Solutions, LLC. Founded in 2010, the company’s mission is to accelerate life science product development and commercialization to biopharmaceutical, medical device, and diagnostic companies by providing clinical, regulatory, and quality compliance solutions. With an array of expertise, our staff understands your unique challenges and concerns faced in a highly regulated environment. We take the time to understand your goals and limitations to provide you the best solutions. Assembling QA and Regulatory professionals with a vast knowledge base ensure that each project is handled with your unique concerns, challenges, goals, and limitations in mind. We understand your environment and what you need to succeed as you navigate the maze of compliance requirements in the pharmaceutical, biotechnology, and medical device industries. Gxp Central, we focus on improving your operations and maintaining compliance in a changing regulatory environment.
    Integrated Project Services
    IPS-Integrated Project Services, LLC is a global leader in developing innovative solutions for the consulting, architecture, engineering, project controls, construction management, and CQV of technically complex facilities worldwide. With technical expertise spanning R&D to pilot-scale to large-scale production, our team specializes in the technology, trends, and regulatory environment to successfully deliver capital projects and improve operations. Headquartered in Pennsylvania, IPS is a multinational company with over 1,700 professionals and 23 offices in 10 countries.
    RJR Consulting
    RJR Consulting, Inc. is a global life sciences regulatory compliance company founded in 2002, serving businesses, organizations and governments around the world. Headquartered just outside of Columbus, Ohio, we have affiliates offices in Brussels, Belgium and Buenos Aires, Argentina with multiple affiliate partners throughout North America, Latin America, Europe, Russia, the Middle East, South Africa and Asia.
    WCG Avoca
    Welcome to WCG Avoca's LinkedIn page! Follow us for company news, product updates, industry insights, and more.Our mission is to have a positive impact on all clinical trials by helping clinical research companies increase quality, ensure compliance, and improve efficiency so that medicines can reach patients faster. The Avoca Quality Consortium, Avoca’s cross-functional collaborative, unites sponsors, CROs, and clinical service providers to address challenges and maximize opportunities to mitigate risk and improve both quality and execution in clinical trials.