Our team of experts helps our clients develop the right strategic solutions by continuously studying emerging best practices, especially in terms of local and international regulations, to provide the best possible solutions.
About Us
Exigence is a life-sciences staffing firm that is been in the industry for over 10 years. We help our clients implement the right strategic solution as we constantly study emerging best practices, in local and global regulations. The fundamental principal of Exigence is to fulfill your staffing needs in an expedited and quality driven manner. At Exigence, we combine the strength of our expertise, experience and high-quality deliverables to advance clinical development, market access and post-approval support to the Pharmaceutical and Medical Device industries. We strive hard to find you the best talent for your needs in regulatory affairs, pharmacovigilance, clinical data management and validation (computer system validation and equipment validation
Our recruiters draw on extensive industry expertise to fully understand your hiring needs and conduct a rigorous identification and screening process to provide a shortlist of highly qualified candidates through contracted resource placement, an alternative to traditional full-time hiring.
Our Services
Regulatory Affairs
Our full range regulatory affairs solutions and services are dedicated to delivering the highest quality support, assistance and regulatory approvals. We follow the needs of our customer and their portfolios, as we work with a wide range of product categories: medicinal products, medical devices, cosmetics, and food supplements.
Pharmaceutical Validation
Our competency is in the pharmaceutical, biotechnology, and medical devices industry with expertise in both traditional and agile processes. The flexible validation services offered are user-oriented, efficient, and scalable to meet the requirements of any size company.Risk management with a risk-based validation approach.
Medical Affairs
Our wide variety of expertise means we will support your organization with world-class Medical Affairs solutions, when you require them in the following streams:
Clinical Affairs
Our experience and expertise means you can personalize your clinical trial operations. From CRAs that are dedicated to your project, a responsive, hands-on senior management team, and a process that’s agile and able to accommodate
Pharmacovigilance
Pharmacovigilance services offered by consist of but are not limited to pharmacovigilance consulting – e.g. benefit-risk analysis, European Economic Area (EEA) Qualified Persons for Pharmacovigilance (QPPV), local QPPV, Safety data exchange agreement