Compliance Companies - Top Pharma Compliance Service Companies

Pharma Tech Outlook: Pharma Tech Magazine

Cutting Edge Information : Taking Charge Of Fmv Compliance

Top 10 Pharma Compliance Service Companies - 2021


In the wake of COVID-19, the pharma sector witnessed a surge in tech-driven innovations built to help the dynamic business arena cope with the disruptions of the pandemic and drive the fastest-ever vaccine development trials in history. With these never-before-seen circumstances causing a widespread digitalization of processes, the pharma compliance space also delivered comprehensive new regulatory mandates to ensure that sensitive information is always stored and transferred securely. And in this evolving market brimming with emerging opportunities pharma compliance solutions and services vendors are helping their clients significantly improve the efficiency and productivity of their compliance operations.

From a technology perspective, the utilization of robotic process automation (RPA) and machine learning algorithms is helping pharma businesses automate cumbersome processes and minimize human execution. Similarly, other solutions that leverage AI, IoT, and blockchain technologies are also helping pharma companies stay abreast of the latest developments in the regulatory channel and quickly move to action in establishing timely compliance.

In order to help organizations steer through the ever-evolving pharma compliance space and find the solution that best suits their needs, a distinguished selection panel of Pharma Tech Outlook has examined and selected the leading-edge pharma compliance solution and services providers and shortlisted the organizations that are leading the charge in resolving the prime challenges in the pharma compliance arena.

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

    Pharma Compliance Service Companies

  • IPS is an EPCMV service provider that incorporates the complete project life cycle in its business process to present the optimum innovative solution to a client’s requirement. Founded in 1989, IPS is an EPCMV service provider that incorporates the complete project life cycle in its business process to present the optimum innovative solution to a client’s requirement. Along with EPCMV, the company also has a competent and robust Commissioning, Qualification, and Validation (CQV) compliance division that efficiently caters to the clients’ compliance needs. From the CQV perspective, the company is constantly seeking out and developing different technologies that can help speed up the drug production process

  • PharmaBioServ is the Life Sciences Industry Leader in regulatory compliance, validation, advanced therapy products, and other regulated industry support services. The company provides services to Pharmaceutical, Medical Devices, Consumer Products, Biotechnology, Advanced Therapies Products industries through out the Globe. WIth 27 years of experience, the company offers an integrated service structure designed to provide complete solutions to their client needs including Project Management, cGMP compliance, Audits, Quality Systems, Remediation, Regulatory Affairs, Qualification and Validation, Contingent Workforce, Personnel Outsourcing, and Training to Pharmaceutical/Biotech, Medical Devices, Food, Cosmetics and related industries. The company's main objective is to enhance the understanding of theoretical and practical elements in these industries by providing the latest skills from well experienced level resources

  • Founded in 2007, was established to accelerate research through the utilization of cutting edge technologies. The company designs tools and platforms that remove roadblocks and make compliance more accessible to the pharmaceutical industry. Be it larger organizations, growing biotechs, or the National Institutes of Health (NIH), works toward providing customized, effective, and appropriate compliance solutions for each client. As one of the world's leading scientific services marketplace, saves time and money and provides access to innovation while maintaining compliance with an organization’s procurement policies

  • Analytical Lab Group

    Analytical Lab Group

    Analytical Lab Group, proud to be part of Element, is an industry leader in the specialty contract lab space and comprises FDA- and EPA-focused laboratories across the United States. Its experts are focused on Helping Protect Life® through infection prevention, with the most comprehensive testing solutions in the antimicrobial, pharmaceutical, medical device, biotech and healthcare spaces. Its facilities are GLP/GMP compliant, FDA registered, DEA licensed and ISO/IEC 17025:2017 accredited

  • Certara


    Certara is the global leader in biosimulation by providing proven modeling & simulation, regulatory science, and scientific value assessment software and services to help our clients reduce clinical trial burden, accelerate regulatory approval and increase patient access to medicines. With their integrated and proprietary end-to-end platform offers drug development and clinical pharmacology strategy, regulatory strategy, writing and submission, as well as HEOR & market access solutions. Certara serves biopharmaceutical and medical technology customers worldwide. Certara works across all therapeutic areas and innovative therapies, including immuno-oncology, rare disease, CNS, respiratory disease, gene therapy, and global health, providing translational solutions from discovery to patient access

  • Charles River Laboratories

    Charles River Laboratories

    Charles River Laboratories International, Inc., is an American pharmaceutical company specializing in a variety of preclinical and clinical laboratory, gene therapy and cell therapy services for the Pharmaceutical, Medical device and Biotechnology industries. The company Charles River provides products and services to help expedite the discovery, early-stage development and safe manufacture of novel drugs and therapeutics. By positioning worldwide the company co-ordinate resources and apply multidisciplinary perspectives in resolving client's product’s unique challenges. the company since its inception, focuses on timeliness and accuracy in every stage of development means client's can count on reliable, reproducible results – every step of their way

  • Clinilabs


    Clinilabs is a global, full-service CRO dedicated to providing a full range of CNS drug development services to pharmaceutical and biotechnology companies. Clinilabs provides first-in-human through end of phase 3 services, with a global core laboratory. It is an alternative to large CROs providing a full spectrum of offerings to meet the needs of our customers world wide. Since 2000, Clinilabs has completed more than 675 clinical trials, and has worked for 15 of the top 20 pharma companies in the world, to contribute to 19 successful new drug applications (NDAs)

  • Medpace


    Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Headquartered in Cincinnati, the company's mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective

  • Parexel


    Parexel is focused on the development of innovative new therapies to improve the world’s health. The company do this by providing a suite of groundbreaking biopharmaceutical development services that help customers across the globe transform scientific discoveries into new treatments for patients. From clinical trial design to regulatory and consulting services to commercial and market access, their therapeutic, technical, and functional ability is underpinned by a deep conviction. Since its inceptiion, the company provide the most comprehensive drug development capabilities of any clinical research organization (CRO) worldwide. With integrated consulting expertise, their global Phase I-IV clinical research programs are designed with the end in mind to navigate regulatory and market access hurdles more smoothly and cost-effectively, from beginning to end

  • Promedica International

    Promedica International

    Promedica International is a a woman-owned corporation, is headquartered in Orange County, California. The company is providing clinical trials for the medical device, biotechnology and pharmaceutical industries. They delivers the quality and consistent results of a large Clinical Research Organization with the efficiencies and responsiveness of a small CRO. They have been involved in more than a hundred device (implantable, surgical and diagnostic), drug and biotechnology clinical research projects in ophthalmology. The company's software and hardware IT capabilities are designed with an eye toward scalability, enabling us to provide individualized options to suit client's trial’s data and information processing need. PMI has a proven track record of delivering quality results, on time and on budget