Veristat

Veristat, Inc. is a clinical research organization based in Southborough, Massachusetts, with additional offices in North Carolina, California, Canada, the United Kingdom, and Taiwan. Established in 1994, the company specializes in providing a range of clinical development services to pharmaceutical, biotechnology, and medical device companies. These services include biostatistics, statistical programming, medical writing, clinical monitoring, project management, and data management. Veristat supports clients through various stages of clinical trials, offering solutions for advanced study designs, predictive modeling, and regulatory submissions. The firm is dedicated to scientific integrity and client focus, fostering long-lasting relationships with a diverse clientele engaged in developing new pharmaceutical products, vaccines, and medical devices.

Patrick Flanagan

CEO and Chairman

5 past transactions

Instat Clinical Research

Acquisition in 2023
Instat Clinical Research specializes in clinical data management and medical writing, offering a range of services to support clinical trials. The company provides comprehensive consulting and advisory services, including design and analysis for clinical studies. Its expertise spans all phases of clinical development, delivering statistical analysis, forecasting, and data management solutions. Additionally, Instat produces detailed reports and offers annual subscriptions to assist clients in making informed decisions throughout the research process.

Scinopsis

Acquisition in 2023
Scinopsis is a medical writing consultancy that specializes in creating documentation for the pharmaceutical, biotechnology, and medical device sectors. The company offers a range of services, including consulting on medical documentation across various therapeutic areas such as aesthetics, anesthesia, cardiovascular disorders, cell therapy, clinical pharmacology, and gastroenterology. By employing qualified scientists and medical experts, Scinopsis provides expertise in the preparation and filing of essential documents, including clinical trial reports and regulatory submissions, ensuring that clients meet their documentation needs effectively.

SFL Regulatory Affairs & Scientific Communication

Acquisition in 2022
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 & Reimbursement/Market Access, Pharmacovigilance, and 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. In addition, SFL has a Swissmedic establishment license, SME-status at EMA and a network of agents in US, Japan, Canada and other countries. Therefore, SFL can act as marketing authorization applicant and MAH in Switzerland and the EU and conduct submissions to FDA, PMDA and Health Canada and other authorities.

SQN Clinical

Acquisition in 2021
SQN Clinical is a specialist biometrics CROs in Europe and is the preferred clinical development partner for many pharmaceutical, biotechnology and animal healthcare companies in the UK, Europe and the rest of world.

Spero Oncology

Acquisition in 2016
Spero Oncology is a clinical research organization focused on the development of oncology products. The company specializes in providing clinical operations support for oncology clinical trials, primarily in Europe, as well as in Australia and New Zealand. By collaborating with Veristat, a full-service CRO with over 20 years of experience, Spero Oncology enhances its capabilities to support pharmaceutical, biotechnology, and medical device firms throughout the clinical trials and regulatory processes. This partnership aims to offer a broader range of services and therapeutic expertise, ultimately assisting in the expedited market introduction of novel therapies.
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