Top Pharmacovigilance Solution Companies in Europe-2021
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Top 10 Pharmacovigilance Solution Companies in Europe - 2021

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At present, the EU is strengthening its drug monitoring capacities through stricter pharmacovigilance (PV) process. Market experts predict that it is due to the rising number of adverse drug reactions (ADRs), the ageing population, and the rising chronic disease burden.

In light of the EU’s evolving regulatory environment, pharma organisations are now trying to ramp up their PV activities. Their focus is now shifting from primarily safety operations to proactive risk management, personalised medicine, and facilitating transparency between pharma, patients, healthcare providers and regulatory agencies. To aid in their efforts, they are turning towards cloud-based solutions, mobile applications, robotic automation, artificial intelligence (AI), and big data analytics. By applying innovative technology automation tools and processes to PV strategies, the foresighted organisations are securing their future in the European pharmaceutical space.

In the wake of such trends in the sector, Pharma Tech Outlook has compiled a list of accomplished pharmacovigilance solution providers most suited for the current market requirements. Equipped with innovative technological capabilities, these pharmacovigilance solution providers are set to transform the pharma landscape. This edition also blends thought leadership articles from subject-matter experts, CIOs, and CXOs, with real-life stories on how the solution providers have enhanced the capabilities of their clients. We hope this issue of Pharma Tech Outlook helps you build the partnership you and your organisation need, to foster a workspace driven by robust and efficient technology.

We present to you Pharma Tech Outlook’s, “Top 10 Pharmacovigilance Solution Companies in Europe – 2021.”

    Top Pharmacovigilance Solution Companies in Europe

    ASPHALION
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    ASPHALION is a leading international scientific and regulatory affairs consultancy founded about two decades ago that has recently launched a new EU Local Contact Network to provide local pharmacovigilance support to any EU country in order to provide its global solutions for the externalisation of pharmacovigilance services, the European Qualified Person for Pharmacovigilance (EU-QPPv) and the Pharmacovigilance System outsourcing. ASPHALION has created its own PV system with a validated PV database, audited yearly by its clients. ASPHALION PV System has successfully been audited in the last 15 years, with 0 critical findings and is ISO certificated with yearly renewal without even a minor finding ... read full profile
    MS Pharm
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    A PV service provider specialized in medical literature monitoring that reviews and monitors local medical journals and widely used global databases and to offer clients a full view of the safety of its products.The assessment of every record that contains information pertaining to an active substance within a product helps PV professionals with precise reports. The reports provide a complete view of information relevant to the risk-benefit considerations of a medicinal product.As a value add to its clients, MS Pharm identifies and reports any potential Individual Case Study Report (ICSR) from a specific patient reported in the literature to deliver data on any possible side-effects caused by a client’s drug product ... read full profile
    Novartis
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    Novartis provides healthcare solutions that address the evolving needs of patients and societies worldwide. The pharmaceutical organization’s current portfolio includes more than 50 key marketed products. Novartis is also a global leader in immunology and dermatology. The company has been transforming the lives of people living with immunologic diseases, focusing on specialty dermatology, rheumatology, autoinflammatory, transplant, and specialty liver diseases where there remain a lot of unmet medical needs. Novartis consistently demonstrates the drive, self-motivation, and eagerness to learn and succeed within the various disciplines offered, including early clinical development or translational medicine, clinical development, regulatory affairs, medical affairs, and commercial strategy and brand marketing ... read full profile
    Qplus Consult
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    Helping pharmaceutical organizations keep pace with these rapid changes and working for both EU Corporate organisations & local affiliates, Qplus Consult understands international as well as company-specific requirements. To meet client expectations and keep up with market trends, Qplus has a team of enthusiastic and experienced consultants who are dedicated to providing optimum service every day and have a vast collective experience spanning decades. . As experts in the field, Qplus Consult also frequently hosts in-company workshops highlighting the implementation of regulatory requirements ... read full profile
    Sympto
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    Sympto is a validated multivigilance database made by CRO compliance experts. From Literature search, ICSR management, signal, and duplicate detection to direct E2B gateway reporting, Sympto® helps teams manage drug safety in real-time, efficiently. With a complete audit trail accessible in a few clicks, safety departments can achieve streamlined worldwide compliance with Sympto ... read full profile
    ADAMAS
    ADAMAS Consulting is an international specialist consultancy offering a full range of independent GCP, GVP, GLP and GMP Quality Assurance and Quality Management services on a global basis. ADAMAS has conducted thousands of GxP audits in more than 70 countries for over 700 international clients, and the company is committed to providing all its clients with the highest level of service in every country
    APCER
    APCER Life Sciences provides comprehensive drug safety/pharmacovigilance, medical information, medical writing, regulatory services, quality assurance and risk management programs to pharmaceutical and biotech companies globally. The company bring medicinal/scientific expertise through its healthcare professionals & physicians and address full pharmacovigilance requirements for North America, UK & Europe markets
    Biomapas
    Biomapas is a functional and full outsourcing solution provider to the global life science industry, with key expertise in Clinical Trials, Regulatory Affairs and Pharmacovigilance. The company has significant presence across the CEE, Nordic and CIS countries thereby offering fast and reliable patient recruitment for Phase I-IV and medical device clinical trials, while regulatory and pharmacovigilance services are provided across 5 continents
    BlueReg
    BlueReg is an international consultancy organisation offering strategic regulatory advice and hands-on outsourcing solutions to life sciences companies through the entire lifecycle of their products – from product development to life cycle management including Early Access Programs. Its clients are small, medium to large sized innovative companies looking to commercialise treatments for unmet needs leveraging broad expertise of the company's internal consultants and a network of international qualified partners
    ELC group
    ELC is a fully-fledged global regulatory partner, working with major pharmaceutical stakeholders for over a decade. From the development stage through to the implementation of clinical trials, completion of product registration, and successful marketing of the product, ELC aligns itself as a strategic partner to help pharmaceutical companies achieve their goals