Top Quality Assurance Services Companies in Europe -2022
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Top 10 Quality Assurance Services Companies in Europe - 2022

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Quality has always been a crucial factor for the safe and efficient production of drugs, which is critical in the current pharma industry that is riddled with low-grade products entering the market. To thwart the manufacturing of subpar drugs and to comply with the ever-evolving regulations, quality assurance has become a top priority for modern-day drug developers. In light of this, pharmaceutical companies are deploying various technologies, including emerging innovations such as AI, IoT, and data analytics, to drive the highest quality in drug manufacturing.

From a technology applicability standpoint, AI-powered tracking systems are supporting the authentication of vital product information on drug packaging, while blockchain is strengthening security across the drug supply chain. Alternatively, IoT devices are improving regulatory compliance through real-time data feeds that simplify the detection of errors across the value chain. The skyrocketing emphasis on quality assurance is also giving rise to contract manufacturing organizations (CMOs) that can support pharma companies in meeting the ever-evolving quality standards and regulatory mandates. In fact, most CMOs are utilising robotic process automation (RPA) to meet stringent quality requirements and drive productivity. Above all, pharmaceutical companies are striding towards high-quality product manufacturing to enhance their reputation, maximise profits, and provide safe and effective drugs to consumers.

In this edition of Pharma Tech Outlook, we bring you the top quality assurance services providers in the pharma industry. We hope this edition will help our readers make the right choices in managing their pharma quality assurance needs and initiatives.

We present to you Pharma Tech Outlook’s “Top 10 Quality Assurance Services Companies in Europe – 2022.”  

    Top Quality Assurance Services Companies in Europe

    AGC Biologics
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    AGC Biologics offers deep industry expertise and unique customized services for the scale-up and cGMP manufacture of protein-based therapeutics, from pre-clinical to commercial production, both mammalian and microbial.Founded in 2018 as a convergence of Japan-based Asahi Glass Company (AGC) Bioscience, Biomeva GmbH (Heidelberg, Germany), and Denmark-based CMC Biologics, AGC Biologics was established with a mission to offer microbial and mammalian cell lines for early-phase processes through late-phase projects and beyond into routine commercial production.

    Read the success story from AGC Biologics

    Promising 100 Percent Compliant and Risk-Free Product Development

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    PharmaKorell
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    PharmaKorell focuses on advising and supporting start-up companies and established pharmaceutical companies in the field of quality management (GMP, GDP) as an external service provider. As a specialized consultancy they can search for suppliers, service providers, contract manufacturers and strategic cooperation partners etc. on customer's demand, without divulging their identity. After determining their requirements and frame conditions in-depth, like time frame, budget, confidentiality requirements, etc. they obtain offers, references and other information for customers, as well as clarifying regulatory and technical possibilities. ... read full profile
    AaMedi
    AaMEDI is a Swiss based International Healthcare company providing sevices and products in the related areas for their global customers. They provide the Swissmedic License applications like manufactuting of pharmaceuticals, production of API's, wholesale of pharmaceuticals with release, wholesale of pharmaceuticals without release, import of pharmaceuticals with release, import of pharmaceuticals without release, export pharmaceuticals, trade abroad and broker activities. They also offer Quality Management Services like setup of quality system and implementation, maintain the quality system, auditing services, site visits etc. They offer also a Documentation Management System (DMS) for the quality documentations consisting ot Audit trail, which is needed for GMP, GDP, GLP and other Quality Dokumentation.
    AZ Biopharm GmbH
    AZ Biopharm GmbH is an independent FDA registered and GLP / GMP / GCP certified analytical laboratory in Berlin. They are a privately held company that operates for 25 years and has many years of experience in the field of analytics. Their focus of of services are pharmaceutical quality control under GMP as well as bioanalytics of preclinical and clinical studies under GLP and GCP. In addition, their independent service company is GMP-certified and has a permit pursuant to § 13 Section 1 and § 72 of the Medicines Law. Their quality assurance system serves to ensure the quality expected by their customers and to enforce their own quality goals and regulatory requirements. The aim is to maintain and constantly improve the very good quality level.
    Cilatus BioPharma Consulting
    Cilatus BioPharma Consulting specializes in the management and services of CMC Development, CMC Regulatory Affairs, Quality Management, Engineering, Validation/Qualification and Manufacturing for biological products. Cilatus supports small, medium and large biopharma companies in strategy development, strategy execution and operations with their fully integrated team of experienced consultants. Over recent years, they have developed deep expertise and continues to show sustained success in the selection, management, contracting and oversight of Contract Development and Manufacturing Organizations (CDMOs or CMOs) in the biotechnology space. They manage and oversee the development work, drug substance manufacturing, drug product manufacturing, analytical testing, labeling, shipping and supply management at contracted CDMOs and CMOs.
    COCIPHARM
    COCIPHARM is a consulting firm, specializing in pharmaceutical development, project management, and quality assurance. It was founded in 2016 by Corinne Ciappara, Doctor of Pharmacy with nearly 30 years of experience in the pharmaceutical industry. Their professionals develop and nurture long-term partnerships with companies in the healthcare sector.
    MARAS
    MARAS has been providing drug regulatory and quality assurance services to the Swiss and international pharmaceutical industry for more than 30 years. They provide customized services that are tailored to the specific goals and needs of the customer so that they can provide fast, efficient and cost-effective solutions. For their clients, they are highly motivated partners who develop appropriate strategies to achieve their common goals also offering a wide range of services for the pharmaceutical industry, including support in Compliance, Reimbursement and Training of staff.
    Pharma Services Oehler GmbH
    Pharma Services Oehler GmbH is an established pharmaceutical service provider and a valued partner for companies from Switzerland and abroad that have questions in the fields of quality assurance, regulatory affairs, market access, pharmacovigilance, reimbursement, food, cosmetics and medical devices. They have been advising and supporting companies in Switzerland and abroad in all matters relating to quality, approvals pharmacovigilance of medicinal products, as well as other related product groups (food, cosmetic products and medical devices) since 1997.
    QBD
    QBD offers worldwide expertise and solutions in the field of quality management, validation, project management & support and regulatory affairs. Since 2011, they have been helping companies in the life sciences, healthcare and cosmetics industries to qualitatively develop and produce products. They offer companies specialized knowledge, expertise and software in the fields of validation, quality assurance, regulatory affairs, project management and clinical solutions. They offer an extensive range of validation services for their client's processes, applications and equipment.
    SFL
    SFL is a leading consultancy providing integrated solutions to pharma, biotech and medtech companies for global and local activities. SFL’s combined in-house expertise and services mirror key functions in a pharma or medtech product’s life cycle: Regulatory Affairs & Regulatory Intelligence, Quality & Supply Chain, Medical Writing, Public Affairs, Market Access, Pharmacovigilance, and Healthcare Compliance. Apart from strategic and operational support of client projects, experienced SFL team members can take over company-internal roles on an interim management base and provide training courses. As a Veristat company, SFL clients also have access to a substantial range of clinical development services such as global clinical operations, biostatistics and programming.