MCRA Competitors

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. AtVeristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Ourscientific 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, ourversatile approach and bold scientific thinking make the impossible possible. Dependon our game-changing expertise and reliable execution for fast results and positiveimpact 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.

Global Pharma Tek is a Global Clinical Research Organisation that provides End-to-End Clinical Services. Global Pharma Tek offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements. Mission: Achieve leadership in services offered through teamwork, cost consciousness and excellence in science and technology. We partner with our clients and collaborate with them in: Clinical Trial Management Clinical Data Management Biostatistics & Statistical Programming Medical Writing Pharmacovigilance Quality and Regulatory Affairs GMP, GLP and GCP Validations Human Resourcing Global Pharma Tek works with most of the top global Pharma, Biotech & Medical Device companies. Our therapeutic experience includes but is not limited to oncology, diabetes, cardiology, ophthalmology, infectious diseases & respiratory system. We offer flexible business models across service verticals based on client needs. We are enterprise-class clinical software and clinical functional services provider, offers unique blend of both clinical trial domain and core IT expertise with thorough understanding of healthcare and pharma industry and regulatory standards. Global Pharma Tek, clinical functional services practice (FSP) enable pharmaceutical and life sciences industry customers realize their vision of safe, effective, and FDA approved delivery of drug at the lowest cost and at the fastest time to market. The executive management team of Global Pharma Tek comprises individuals who have a proven track record with regard to providing services to Pharmaceutical, Biotechnology, Device and Consumer Health industries. Global Pharma Tek has headquarters in New Jersey (USA) and has offices located in Canada, UK, UAE and India. Visit www.globalpharmatek.com to learn more about our services.

AXIS Clinicals Limited is one of the most experienced and fastest growing Clinical Research Organization. Our state-of-the-art facilities houses 500+ dedicated full-time professionals to ensure the quick turn around time with high quality. Our facilities are accredited by DCGI (Drugs Controller General – India), NABL (National Accreditation Board for Testing and Calibration Laboratories - ISO 15189:2003) and inspected by US-FDA, UK-MHRA, Brazil-ANVISA, France –AFSSAPS / ANSM, GCC, MCC-South Africa etc. Within short span, we have achieved the milestone of completing 2750+ clinical studies and 1000+ product approvals from various regulatory agencies. 65+ regulatory audits from global competent authorities is testament to our professionalism and dedication to quality studies. Our Phase II – IV capabilities are growing along with an extended portfolio of Site Management, Medical Writing, and Data Management.