Smooth Drug Development offers a full range of clinical trial, drug registration and post-marketing services, including consulting, development of registration strategy, conduct of clinical studies and pharmacovigilance in Europe and Asia. We cover wide geography: -Russia -Ukraine -Belarus -Kazakhstan -Latvia -Lithuania -Estonia -Serbia -Slovakia -Hungary -Germany -Spain Our company implemented the principle of "one stop service" when all activities from planning to product registration are performed consistently under the control of a team of professionals. According to the requirements of ISO 9001:2015, in case of outsourcing of vendors we manage their activities as our ones and are fully responsible for the results. Our Clients are leading pharmaceutical, biotech and R&D companies located in Europe, US, CIS and Asia-Pacific region. We offer drug development services: -Consulting center -Pre-clinical research -Clinical trials -ePRO -eTMF/eISF -Drug registration -Post-marketing surveillance -Pharmacovigilance -Training center We are experts in clinical services: -Project management -Medical writing -Feasibility and site selection -Regulatory support -Data management -Logistics and storage -Clinical monitoring -Medical monitoring -Pharmacovigilance -Bioanalytical and central laboratories -Biomedical statistics -Clinical study report -GCP audit Smooth Drug Development has unique IT solutions for clinical trials which help to speed up clinical trials processes and daily activities. Smooth CTMS includes the following modules: -EDC/eSource/IWRS -eTMF/eISF -ePRO -Learning / QMS -Personal Folder -Clinical Monitoring Smooth Drug Development has been ISO certified: -ISO 9001:2015 Quality Management Systems -ISO 27001:2013 Information Security Management Systems -ISO 22301:2019 Business Continuity Management Systems Please contact us at bd@smoothdd.com to learn more about Smooth Drug Development capabilities.
View Top Employees from Smooth Drug Development, next generation e-CRO in Europe and AsiaWebsite | http://smoothdd.com/ |
Revenue | $17 million |
Employees | 46 (36 on RocketReach) |
Founded | 2008 |
Address | Centerville Road Suite 400, Wilmington, Delaware 19808, US |
Phone | +7 812 913-04-23 |
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Industry | Pharmaceutical Manufacturing, Manufacturing General, Clinical trials phase I-IV, IIR, NIS, Manufacturing, Patent protection, Bioequivalence studies, Strategic marketing, Drug dossier preparation/drug registration, Regulatory support/CTA, Pharmacovigilance, Bioanalytics, Animal studies, CRO in Russia, Post-marketing surveillance |
Web Rank | 9 Million |
Keywords | Smoothdrug, Степана Разина 9, Smooth Drug Development, Smooth Clinical Trials, Смуз Драг Девелопмент |
SIC | SIC Code 283 Companies, SIC Code 28 Companies |
NAICS | NAICS Code 32541 Companies, NAICS Code 3254 Companies, NAICS Code 325 Companies, NAICS Code 32 Companies |
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The Smooth Drug Development, next generation e-CRO in Europe and Asia annual revenue was $17 million in 2024.
Julia Sardaryan is the Corporate Development Director of Smooth Drug Development, next generation e-CRO in Europe and Asia.
36 people are employed at Smooth Drug Development, next generation e-CRO in Europe and Asia.
Smooth Drug Development, next generation e-CRO in Europe and Asia is based in Wilmington, Delaware.
The NAICS codes for Smooth Drug Development, next generation e-CRO in Europe and Asia are [32541, 3254, 325, 32].
The SIC codes for Smooth Drug Development, next generation e-CRO in Europe and Asia are [283, 28].