Top 10 Clinical Trial Management Consulting Service Companies in Europe - 2019
pharmatechoutlook
TRILOGY Writing & Consulting: Quality- Driven Medical Writing

Top 10 Clinical Trial Management Consulting Service Companies in Europe - 2019

For several decades, researchers have emphasised the need for large, randomised, and controlled trials to bring out the highest level of evidence that would help them come to an inference for their clinical trials. Most often than not, many trails fail to deliver the desired result due to the lack of a practical, structured, and business-like approach to trail management. Meanwhile, clinical trials are intertwined with potential risks in communications and management, as various stakeholders are involved in performing the trials. At this critical juncture, pharmaceutical centres must have an inherent responsibility and obligation to conduct and manage clinical trials while preserving a high level of quality. To mitigate this impediment healthcare professionals are seeking for eminent clinical trail management service providers who can guide them beyond the advisory level and bring in the optimal solutions.

To help pharmaceutical organisations partner with the best service providers in the industry, Pharma Tech Outlook has compiled a list of top 10 clinical trial management services in Europe/UK. Equipped with innovative technological capabilities and robust offerings, the enlisted companies are constantly proving their mettle in the pharmaceutical sector. To further substantiate the technological advancement in clinical trial management, CIOs working in the industry have penned their insights about new innovations, industrial happenings, and their advice to the aspiring CIOs seeking for it.

We present to you Pharma Tech Outlook’s “Top Clinical Trial Management Service in Europe.”

Top 10 Clinical Trial Management Consulting Service Companies in Europe

3S Pharma is a Germany-based company conducting innovative, safe and scientifically-proven clinical trials to help its customers get regulatory-compliant products within a short timeframe. Started in 1996, 3S Pharma’s CRO & CMO services also comprise bioequivalence/bioavailability studies, pharmacokinetic profiles, drug-drug interactions, pain assessment studies, and more. As one of the top clinical trial management consulting/service companies in Europe, 3S Pharma has several achievements to its credit. Among those successes, 3S Pharma-developed highly standardised procedure of tablet crushing and underultrasound controlled injectable products, surely deserve a special mention. 3S Pharma is also developing a technique to assess the distribution on the mucosa of the intra-nasal administered products

3spharma.eu

Today, as the success of a trial depends on the service provider’s proven experience in conducting international studies, dealing with global trial complexities, and managing operational, regulatory and coordination challenges, CSM brings over two decades of strong expertise in managing Direct-to-Patient studies, and working with many trial sponsors, couriers, and clinical sites. CSM makes clinical trials more cost-efficient and reliable with specialised services like On-Demand packaging and labelling, Direct-to-Patient shipping, QP services, and biological sample management. One key aspect that truly differentiates CSM from its competitors is its innovative On-Demand services. With CSM’s On-Demand method, its partners are able to shorten trial timelines, reduce clinical trial costs, increase the flexibility of drug discovery study, and tackle any packaging and labelling difficulties

www.csmondemand.com

A leading Polish contract research organization (CRO), Clinmark is empowering clinical studies in Central and Eastern Europe (CEE) with its clinical trial management services, consultancy, and training. Since 2001 it has been organising, conducting, and supervising the management of clinical trials phase I to IV as well as non-interventional studies. In addition to that consultancy in the area of system management, audit and inspection constitute an important part of their business. Clinmark’s team advises pharmaceutical companies on formulating clinical trial designs, optimising internal procedures, and conforming to regulatory compliances

clinmark.pl

Germany-based CRS offers a complete range of high-quality clinical development and consulting services to companies operating in pharmaceuticals, biotechnology, and medical devices industry. Aside from clinical conduct of trials, CRS’ portfolio includes services for project management, quality assurance, clinical trial supply management, medical writing, among others. To bolster its services, the company has a core focus on patient recruitment for specific areas, which includes metabolic disorders such as diabetes, obesity, and associated cardiovascular complications, along with renal and hepatic impairment. Additionally, the company’s geographical location and research sites across Germany enable clients to have access to patients from varying demographics, allowing CRS to perform multicenter trials under one service agreement

crs-group.de

Marti Farm, a company based out of Zagreb, Croatia, is a contract research organization supporting the needs of the pharmaceutical, biotechnology, medical devices, food supplement and cosmetics industries across a variety of core services areas. The company is internationally recognized as a reliable partner and provider of consultancy and regulatory services with proven track record of 8+ years. The Marti Farm team has developed a fully validated and user-friendly pharmacovigilance safety database known as Sympto®, which has been designed to improve case reporting, literature searching, and qualitative signal detection. Marti’s core belief is continuous personal development aimed at strengthening its expertise and approaches in order to drive added value for its clients from both the operational and the strategic aspects

www.martifarm.hr

Trilogy is a medical writing consultancy. The company works proactively with its clients to plan, coordinate and write their clinical documentation to meet aggressive timelines, with a readability that reduces the time for review and approval. Trilogy covers all clinical areas and helps its clients in the areas of increasing the speed and e¬ffectiveness of their clinical documentation, time to submission to database closure of the final study, writing dossiers, and studying report. The company offers industry-level training to budding medical writers and brings a unique blend of seasoned medical writers and their experience to the table

www.trilogywriting.com

TriTiCon is a clinical trial management provider that offers strategic consultancy expertise in the area of clinical data handling, TriTiCon is dedicated to helping pharmaceutical and biotech companies, CROs, start-ups and tech providers navigate through these changes. The company’s skilled consultants have over two decades of experience in clinical research and act as the “missing piece” in the client's resources and competences. The company assists clients in solution implementation, lead validation, testing, writing the SOPs, and performing training to fill any gaps

www.triticon.com

proinnovera

proinnovera

Founded in 1997, proinnovera is an independently-owned Clinical Research Organization (CRO), which is specialized in dermatology. The company offers its therapeutic expertise on dermatology, oncology, and inflammatory diseases. The company covers the full spectrum of services for a dermatological CRO in pharmaceutical contract research. The company’s outstanding network of recognized dermatological study sites and KOLs guarantees high patient recruitment numbers all over the world. proinnovera constantly contributes to cancer research and develops a strong awareness of the complexity of this type of research. The company also possess excellent experience in inflammatory diseases, which can assist with the conduction of dermatology study projects

SanaClis

SanaClis

Founded in 2000, SanaClis is a full-service European CRO, which offers a comprehensive range of services for clinical trials. The company holds the experience of delivering studies for various sized sponsors, starting from virtual biotech. The company has in-house logistics capabilities, which include QP services, customs brokerage, warehousing and distribution, and sourcing of clinical trial materials, comparators and rescue medication. SanaClis offers various services such as regulatory, clinical monitoring, IP & CTS Management, customs clearance & brokerage, site contracting & payments, quality management, data management, and pharmacovigilance

SMO Group

SMO Group

SMO Group is an acknowledged clinical trial logistics provider, offering the complete range of logistics services for clinical trials while ensuring the highest standards of operation. Through its profoundly experienced and qualified personnel, SMO Group is fully versed in global procedures of clinical trials, and at the same time, has comprehensive local expertise, which ensures efficient operation and full adaptation to local necessities. Side by side with widespread local expertise and affordable solutions, SMO Group provides legal and consultancy support aimed at ensuring a successful study start-up