Our Business Partners are offering BaseCon's product portfolio in order to be able to offer their clients excellent services.This list is not all-inclusive:
Virtual PV was launched in 2012 to provide a complementary range of services centred on pharmacovigilance and medical information. Their aim is to help Clients advance practice, respond effectively to new regulatory requirements, and resolve capacity issues. The lead services currently revolve around implementing PV risk management, supply of PV and medical information Apps for smart devices, helping Clients with preparations for the new PV legislation, and provision of case management.
Clinquest is a global provider of medical development services to the pharmaceutical, biotechnology, food and medical device industries. Clinquest delivers innovative and sound clinical trial and development solutions – from “first-in-human” studies through post registration surveillance. Clinquest has a 10-year history of serving customers, both large and small, and with a diversity of compounds and devices. The focus is on strategic development, medical trial expertise, operational management and analysis of projects that support clinical development, from product selection to Phase I-IV clinical studies.
Cyncron is a full-service clinical contract research organisation with extensive experience from working in many therapeutic fields, including cardiovascular, diabetes and oncology research. Cyncron offers clinical operations, biometrics, medical affairs, pharmacovigilance, quality management and consultancy services to both national and international clients. Cyncron headquarters are in Denmark and with offices in Sweden and Finland, Cyncron operate in the Nordic countries. Through partnership Cyncron also satisfy requests for services in other countries. Founded in 1985, Cyncron has a long track record with strong liaisons in academia and the biotech and pharmaceutical industry.
CPI is a young and dynamic, independent contract research organization (CRO) located near Bonn, Germany. They provide a full range of clinical development services to biotechnology, pharmaceutical and medical device clients from Phase II to Phase IV. Their key focus is the delivery of a continuous stream of quality data, at the same time achieving targeted enrollment, and respecting project timelines and budget goals. Their service quality is maintained by strict adherence to ISO 9001:2008 standards at every level of the company.
Lindeq was founded July 2004 by medical docters and experts with extensive experience from the pharmaceutical industry and as independent PV consultants. Our key values are Knowledge, Quality and Efficiency. No task is too small or too big and our aim is to always provide the necessary resources at the right time. We promise always to deliver on time and with our key values intact. Since the foundation, Lindeq has expanded the network of consultants and experts within several fields, among them pharmacovigilance, drug safety, quality assurance, metrics, risk management, computer validation, and human factor. The Human factor approach is a very important cornerstone in our work.
Prism puts clinical excellence at the forefront of medical marketing. Due to itsteam of physicians and scientists, many of whom have extensive experience within the pharmaceutical industry, Prism can provide seamless support fromdrug development to commercialisation. Established in 2001, Prism has delivered projects for a global client base of around 40 different pharmaceutical companies.
TAKE Solutions' leading edge technology enables companies across industry verticals to achieve business efficiencies. TAKE’s competitive advantage is its knowledge-based approach, high product IP, global reach, and long track record of success. With more than 800 current employees, TAKE Solutions’ world headquarters are in Chennai with U.S. headquarters in Princeton, NJ
UBC (former HPM Geneva) is an independent contract research organisation offering services in the areas of drug safety and medical writing.Their dedicated teams of physicians, pharmacists and scientists provide a full range of services in these areas tailored to meet the specific needs of our clients. Their drug safety team provides fully integrated drug safety services including the access to SafetyBase Interchange and additional BaseCon products. Their team of experienced medical writers offers a range of services for regulatory bodies and for publications and congresses.
Vigilex was established in 1996 by Dr Maria Koster, PhD who from the start is CEO of the Vigilex Group. Vigilex was the first full-service Contract Safety Surveillance Organisation (CSO) in Europe, providing a broad range of products and services in pharmacovigilance and vigilance of medical devices. Worldwide based pharmaceutical, veterinary and medical device industries increasingly rely on our specialist expertise. Strategic alliances with expert partners strengthen our capacity to consistently develop global services. Our Quality Assurance department ensures that all products and services are delivered in concord with national and international requirements. Since 2001, Vigilex is NEN-ISO 9001 certified.