Ensuring the integrity and safety of clinical trials is paramount. Discover how our DMC Services, powered by our deep biostatistical expertise, deliver precision and reliability in every data analysis. Learn more > https://hubs.li/Q02Gw9N-0 #DMCServices #Biostatistics #ClinicalTrials
About us
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at talentacquisition@veristat.com. Be vigilant.
- Website
-
http://www.veristat.com
External link for Veristat
- Industry
- Research Services
- Company size
- 501-1,000 employees
- Headquarters
- Southborough, Massachusetts
- Type
- Privately Held
- Specialties
- Strategic Consulting, Safety Management, Data Management, Biostatistics, Statistical Programming, Project Management, Medical Writing, Regulatory Submissions, Adaptive Clinical Trial Design, Site Monitoring, Regulatory Consulting, Clinical Trial Patient Recruitment, Clinical Trial Data Standardization, Clinicl Trial Design, Clinical Trial Management, US Regulatory Agent, Pharmacovigilance, Marketing Applications Support, IND Support, Regulatory Publishing, Biologic, Gene Therapy, Full-service CRO, and Oncology Clinical Trials
Locations
Employees at Veristat
Updates
-
Navigating medical writing for rare disease therapies 🛣️ Learn how we helped a global pharma company overcome medical writing challenges for their rare disease therapies. Download the case study 📩 https://hubs.li/Q02Gw6YV0 #MedicalWriting #RareDiseases
-
Take your talent resourcing strategy to the next level! 💻 Our blog highlights how FSP resourcing can help navigate talent shortages and shrinking timelines. Read now > https://hubs.li/Q02Gw6T80 #biopharma #biotech #clinicaltrials
FSP/Resourcing: Meeting the Moment with Expert Resources
veristat.com
-
Regulatory intelligence (RI) is increasingly crucial for global product development and market access in key regions. Our RI team analyzes regulations and the competitive landscape to provide you with strategic insights that maximize your success. Learn about Regulatory Intelligence support > https://hubs.li/Q02GvYNQ0 #RegulatoryIntelligence
Commericalization - Regulatory Intelligence | Veristat
veristat.com
-
Flawless submissions and global regulatory success – that's what Veristat offers. See how we’ve helped companies overcome challenges and reach milestones. Download now 📩 https://hubs.li/Q02Gw3ZG0 #Regulatory #ClinicalTrials
-
As the industry continues to adopt a patient-centric approach, the use of real-world data is becoming increasingly essential in informing drug development and regulatory decision-making. Read about the FDA's guidance on Patient-Focused Drug Development (PFDD) to enhance your product development and regulatory decision-making👇 https://hubs.li/Q02Fw4sQ0 #PFDD #DrugDevelopment #patient
-
The EMA published information material for accelerating the clinical trials in the EU initiative (ACT EU). This includes: 📍Map of national projects supporting non-commercial sponsors at the national level 📍Webpage with detailed information on the stakeholders and groups within the European Medicines Regulatory Network (EMRN) Read more > https://hubs.li/Q02FwbVy0 #clinicalresearch #clinicaltrials #CTIS
ACT EU Information on National Projects and Stakeholder Network
accelerating-clinical-trials.europa.eu
-
Hear from our CCO, Rachel Page, as she joins Sterling Bay's webinar as a panelist to discuss 'A Triangle Perspective on AI, ML, & the Future of Drug Development.' The panel will address how AI/ML developments are revolutionizing the global biopharmaceutical industry. Register today 👇 https://hubs.li/Q02F-yM-0 #globalbiopharmaceutical #DrugDevelopment
-
The FDA issued draft guidance on essential drug delivery outputs for devices intended to deliver drugs and biological products. The guidance: 👉 Targets combination products 👉 Aims to streamline device development 👉 Offers recommendations on design outputs 👉 Informs drug delivery performance Stakeholders may submit comments on the draft by 30 September 2024 > https://hubs.li/Q02FwgPl0 #IVDs #medtech #regulatoryaffairs
EDDO for Devices Intended to Deliver Drugs and Biological Products
fda.gov
-
Facing staffing reductions in Biopharma? Discover how strategic FSP resourcing can help Biotech firms navigate talent shortages and achieve clinical trial success. Read now 👉 https://hubs.li/Q02F-yMb0 #biopharma #biotech #clinicaltrials
FSP/Resourcing: Meeting the Moment with Expert Resources
veristat.com