SymGet Technologies LLC
Pharmaceutical Manufacturing
New Jersey, United States
31 employees
- Employees
- 31
SymGet Technologies LLC Overview
- Headquarters
- New Jersey, United States
- Website
- symgettech.com
- Industry
- Pharmaceutical Manufacturing
- Employees
- 31
- Founded
- 2016
- NAICS
-
Pharmaceutical and Medicine ManufacturingMedicinal and Botanical ManufacturingPharmaceutical Preparation Manufacturing
About SymGet Technologies LLC
SymGet Technologies is backed by years of collective intelligence of its founding partners and works with renowned pharmaceutical companies and marketing authorization holders in various parts of the world. SymGet provides end-to-end statistical analysis services to pharmaceutical companies for global clinical trials and BA/BE studies. More importantly, SymGet comprehensively consults to biotech and pharmaceutical companies across the globe to help them constantly evolve their study design for pre-clinical and clinical studies to be in line with the regulations pertinent to their potential market launch. SymGet has brought together a panel of senior medical writers and a robust team of biometrics professionals to build a formidable combination that provides high quality analytics consulting and analytical services to pharmaceutical companies, research organizations and health agencies. SymGet provides clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; data management, statistical analysis, project management, clinical monitoring, medical writing, and vendor management. From clinical trial design to regulatory and consulting services and choice of right GMP manufacturing partners, our therapeutic, technical, and functional ability is reinforce by a deep conviction in what we do. We cater below services with unparalleled quality from the USA and the India; - Contract research: Phase I to IV Clinical Trial (Clinical Operations, DM, Medical Writing, Biometrics - using licenced version of SAS) - Consulting: Independent audits (GCP and GMP), Selecting vendors for GMP, FDA, EMEA approved manufacturing plants, vendors for clinical trials, selection of CRO etc - Staffing (all level): Corp to Corp and Referral basis - Training: SAS Base, SAS Advanced - Clinical, Data Management, Clinical Research Associate.
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