Top Pharmacovigilance Consulting/Service Companies in Europe
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Top 10 Pharmacovigilance Consulting/Service Companies in Europe - 2020

As the battle to combat the increasing incidence of lifestyle diseases and other non-communicable disease wages, the medical and pharmaceutical sciences shifted gears bringing forth a plethora of medicines to tackle disease states effectively. On the flip side, adverse reactions to drugs are becoming an all too common problem, and it is crucial to monitor and assess the safety of drugs. Pharmacovigilance has never been more vital to enhance patient safety and maintain compliance.

The pharmacovigilance market is striving to detect and manage emerging safety risks by incorporating cutting edge technologies to guarantee patient safety, lessen costs, and meet regulatory compliance. Pharmacovigilance focuses on adverse drug reactions and drug toxicity, and there is continuous innovation for a well-organized system to monitor and assess the safety of medicines. Companies are implementing technologies like artificial intelligence, analytics, blockchain, and cloud to digitize and optimize drug safety and development. The pharmacovigilance arena is also witnessing innovation in designing digital solutions to address evolving issues related to drug safety and process consistency and impart seamless integration of safety data from disparate sources.

Against this backdrop, there are various service providers in the industry with a set of advanced and integrated pharmacovigilance services. To help companies navigate through the best-of-breed pharmacovigilance service providers, Pharma Tech Outlook has compiled a list of “Top 10 Pharmacovigilance Consulting/ Service Companies in Europe-2020.” The enlisted organizations are transforming pharmacovigilance operations and processes by incorporating cutting edge technologies. We hope this edition of Pharma Tech Outlook helps you build a partnership to boost productivity and efficiency.

We present to you Pharma Tech Outlook’s “Top 10 Pharmacovigilance Consulting/Service Companies in Europe - 2020.”

Top Pharmacovigilance Consulting/Service Companies in Europe

Marti Farm is a fast growing CRO with the required expertise for providing successful, efficient support to meet the individual needs of our clients and partners worldwide. The company is highly valued as an expert by its clients and partners on the East Adriatic Region and other EU and non-EU markets. Based on its global network of providers, Marti Farm performs highest-quality services on the market, while ensuring that customers’ business needs are fulfilled quickly and efficiently. At its core, the company delivers a multi-client, web-based safety database and pharmacovigilance solution, Sympto®.

www.martifarm.hr

MS Pharm provides extensive support to MAHs in the pharmacovigilance (PV) space worldwide by monitoring the local and global literature. The company utilises its premium processes with automatic steps, involving validated tools, and proficient team of reviewers to offer a full range of relevant information on PV from local literature sources. With the mission to bring deep local knowledge and insights from local experience to the MAHs so that they can benefit from them, the Prague-based firm leaves no stone unturned. MS Pharm constantly upgrades its software and adds new functionalities to provide up-to-date, cost-effective, scalable solutions to its customers

www.mspharm.eu

As a full service and independent consultancy firm, Qplus consult brings to the table years of experience in medicinal products, medical devices, food supplements and cosmetics for supporting clients with GxP and ISO quality management, pharmacovigilance, medical writing, medical communication, regulatory and medical affairs, auditing and training. Qplus consult keeps a close tab on the sea change occurring in the realm of pharmacovigilance. From smarter collection and reporting of safety reports of suspected adverse reactions to the assessment of on market performance of medicines and improved engagement between patients, regulators and healthcare professionals are critical elements. At the core, Qplus consult specialises in pharmacovigilance for human medicinal products, materiovigilance, cosmetovigilance, and nutrivigilance

www.qplusconsult.com

AtoZ-CRO

AtoZ-CRO

AtoZ-CRO GmbH is a German full-service clinical research organization. We provide comprehensive outsourcing solutions to the global life science industry. The company has more than 35 years expertise in Clinical Studies, Monitoring, Regulatory, Pharmacovigilance and Biometry on a national and international level. AtoZ-CRO GmbH has significant presence in Western- and Eastern-Europe, here offering a state-of-the-art Early Phase Unit as well as fast and consistent patient recruitment. The company serves clinical trials for pharmaceuticals and radiopharmaceuticals (Phase I – IV), medical devices, nutritionals and cosmetics. Our highly flexible, qualified and motivated staff advances all customer projects with high quality, short communication ways and a quick decision making

CLINMARK

CLINMARK

A leading full-service CRO specializing in clinical research and global clinical consulting since 2001. Clinmark is committed to providing support for pharmaceutical and biotechnological companies in the area of research and development through operational activities, professional auditing, consulting and education.8 out of top 10 worldwide pharmaceutical companies are our clients.We combine operational activity in clinical research, professional consulting and education. This unique combination of related areas of activity creates synergy, which offers an advantage for our clients and delivers measurable impact on providing professional services for clinical research and optimizing its conduct in terms of time and cost

ELC Group

ELC Group

Global regulatory partner, working with major pharmaceutical stakeholders from the development stage through to the implementation of clinical trials, completion of product registration, and successful marketing of the product.pharmacovigilance (PV) solutions enable bio/pharmaceutical companies to meet their postmarketing PV obligations in a robust, cost-effective and compliant manner. All our PV solutions are compliant with the guidelines of the European Medicines Agency (EMA), Food and Drug Administration (FDA) and International Conference on Harmonisation (ICH)

Oxon Epidemiology

Oxon Epidemiology

OXON provides global safety and pharmacovigilance consulting services to enhance patient care and patient safety in relation to the use of medicines and acquiring reliable information for the effective assessment of the risk-benefit profile of medicines. Helps audit drug safety procedures and provide appropriate risk management plans to manage your product safety programme

PharmaCqAre

PharmaCqAre

PharmaCqARE set up Pharmacovigilance Systems tailored for the structures or for the countries, to allow the surveillance of the approved products, to prevent any risks of adverse drug reactions resulting from their use, and implements data collection, recording and evaluation processes. PharmaCqARE follows up any local identified signals up to product information update and makes proposal of product information update in case of confirmed signals.PharmaCqARE prepares or reviews any reports including PSUR (Periodic Safety Update Report), PBRER (Periodic Benefit Risk Evaluation Report), the DSUR (Development Safety Update Report) and RMP (Risk Management Plan)

Q-People

Q-People

Q-People implements and improves quality management systems. We help companies validate processes, procedures and systems. We provide targeted talent and sourcing solutions to all domains in the life sciences sector, from Health Care and Pharmaceutical to Biochemistry and Cosmetics.Provides targeted solutions in Quality and Compliance projects in the Life Sciences sector, from Pharmaceutical and Biotech to API and Medical Device Production

QVigilance

QVigilance

QVigilance is a Pharmacovigilance (PV) Service Provider that offers comprehensive PV and risk management services for Sponsors of clinical trials and Marketing Authorisation Holders. Use our pharmacovigilance services and expertise to meet all your clinical trial and post-authorisation needs as you remain compliant with your regulatory obligations and safeguard your patients and trial subjects through proactive continuous safety monitoring and proportionate risk minimisation of your medicinal products