Global Pharma Tek

Major Drugs - Edison, New Jersey, US

Global Pharma Tek Details

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.

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Employees: 248
HQ: (732) 543-7155
Location: Edison, New Jersey, US
Revenue: $45.2 million
Clinical Research Clinical Development Clinical Trials Medical Writing Pharmacovigilance Clinical Data Management Regulatory Affairs
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