Scandinavian CRO
Tillverkning av läkemedel
Our vision is to help our clients perform better clinical research. Improved quality, design and speed at every step.
Om oss
Scandinavian CRO is a privately held, full-service Contract Research Organization (CRO) with offices in Uppsala and Gothenburg. SCRO is headquartered in Uppsala, Sweden and covers Sweden, Norway, Finland and Denmark. We perform complete clinical studies or parts of projects within clinical research, both for pharmaceuticals and medical devices. If you want to hire a consultant, you can choose between various specialists such as project managers, clinical research associates, administrators and research nurses. Let us support you with navigating the national and international laws and regulations governing clinical trials and all the issues related to it. You will naturally always be in control and have oversight of your study, but we are happy to do the work for you, whether you need a consultant, custom services, or a full-service solution. If you want to use us as an intellectual resource or sounding board, we are happy to share our expertise with you. We have extensive experience with Phase I to IV clinical trials in a wide range of therapeutic areas: Cardiology, Oncology, Urology, CNS, Endocrinology, HIV, Gastroenterology, Anaesthesia, and many more. We would love to meet you. It all begins with a conversation. Contact us. Phone: 46 - 18 10 05 50
- Webbplats
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http://www.scro.se
Extern länk för Scandinavian CRO
- Bransch
- Tillverkning av läkemedel
- Företagsstorlek
- 11–50 anställda
- Huvudkontor
- 750 15 Uppsala
- Typ
- Privatägt företag
- Grundat
- 2007
- Specialistområden
- Project Management, Biostatistics, Data Management, Monitoring, Feasibility and site selection, Medical Writing, RA and EC submission, Pharmacovigilance, MedCenter, Regulatory services, GCP training, Clinical Research, Clinical study, Clinical trial, Medical device, Pharmaceuticals, Clinical drug development, Clinical operations, Outsourcing och Clinical monitoring
Adresser
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Primär
Skolgatan 8
P.O. Box 150 27
750 15 Uppsala, SE
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Life Science Center Espoo
Helsinki, FI
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Oslo
Oslo, NO
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Copenhagen
Copenhagen, DK
Anställda på Scandinavian CRO
Uppdateringar
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What do you have planned after the summer? Are you planning to start a clinical study? Whether you work with pharma, ATMPs or medical devices, we can support you with a range of start-up activities to ensure a successful clinical study start-up. We would love to hear from you to discuss your needs. Visit us at scro.se #clinicalresearch #clinicaltrials #clinicalstudy #ATMP #biologic #pharma #medicaldevice #IVD
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Does your company fulfill ICH-GCP criteria for Sponsor oversight? According to ICH-GCP: The sponsor should ensure oversight of any trial-related duties and functions carried out on its behalf, including those subcontracted to another party by the sponsor’s contracted CRO(s). Many pharma and medical device companies do not have the resources or adequate employee competence to conduct full oversight of their contract research organizations (CROs). With an experienced Oversight Project Manager from Scandinavian CRO (SCRO), the Sponsor can meet the GCP oversight criteria and ensure tight communication with the CRO throughout the study. Contact us to find out how we can support your company to ensure adequate ICH-GCP oversight. https://scro.se/contact/ #ichgcp #sponsoroversight #clinicalresearch #clinicaltrials #projectmanagement #clinicalprojectmanager #oversightPM
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Scandinavian CRO omdelade detta
Do you need experienced consultants for your clinical projects? Whether you need part-time or full-time consultants, we offer flexible solutions that fit your needs. We provide experts with the right knowledge & experience - so they can quickly become valued members of your team. Contact us at scro.se to find out how our experts can support you with your clinical studies. #clinicalprojectmanager #clinicalresearchassociate #clinicaltrials #pharma #atmp #biologics #medicaldevice #clinicalstudy #norway #sweden #denmark #finland #consultants
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Are you looking for a contract research organization (CRO) to help you design and conduct your clinical trial? Scandinavian CRO (SCRO) is a full-service CRO offering services that support your clinical research. If you’re currently developing a pharmaceutical, medical device, IVD or biologic, let our team provide you with the expert support that you need to succeed in your clinical studies. Watch our video to learn about the top reasons why our customers choose SCRO. #pharma #clinicaltrials #biologics #medtech #IVD #medicaldevice #clinicalresearch #clinicalstudies #clinicaldevelopment #Contractresearchorganization #Scandinavia #clinicalresearchassociate #clinicalprojectmanager
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Ulrika Hammarström awarded Uppsala County's Entrepreneur of the Year Recently, Ulrika Hammarström, CEO and Founder of Scandinavian CRO (SCRO) was awarded Entrepreneur of the Year in Uppsala, Sweden. Last week, local winners of this award from around the county gathered at Uppsala Castle where Ulrika was awarded Entrepreneur of the Year for Uppsala County by the County Governor, Stefan Attefall. According to the jury, Ulrika has distinguished herself by her leadership in creating a workplace that employees are proud of, as well as promoting local businesses and working for the socially vulnerable through volunteer work and financial contributions. During the awards ceremony, Jenny Laev Alfvén was awarded Young Entrepreneur of the Year in Uppsala County. Every year, Företagarna | Swedish Federation of Business Owners awards entrepreneurs at the local, regional and national level who make positive contributions to society that are above and beyond. As regional winners, Ulrika and Jenny will represent Uppsala County at the national finals in October. #åretsföretagare #leadership #awards #kudos #celebratesuccess #proudmoment #contractresearchorganization #clinicalresearch #enablinghealth https://lnkd.in/deDXYvdi
Här är Årets Företagare och Årets Unga Företagare i Uppsala län
foretagarna.se
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Scandinavian CRO omdelade detta
Does your company fulfill ICH-GCP criteria for Sponsor oversight? According to ICH-GCP: The sponsor should ensure oversight of any trial-related duties and functions carried out on its behalf, including those subcontracted to another party by the sponsor’s contracted CRO(s). Many pharma and medical device companies do not have the resources or adequate employee competence to conduct full oversight of their contract research organizations (CROs). With an experienced Oversight Project Manager from Scandinavian CRO (SCRO), the Sponsor can meet the GCP oversight criteria and ensure tight communication with the CRO throughout the study. Contact us to find out how we can support your company to ensure adequate ICH-GCP oversight. https://scro.se/contact/ #ichgcp #sponsoroversight #clinicalresearch #clinicaltrials #projectmanagement #clinicalprojectmanager #oversightPM
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The critical role a CPM plays in your clinical study Clinical Project Managers (CPMs) lead project teams in planning and carrying out clinical studies. The CPM closely collaborates with the project team to solve challenges as they arise and drive the clinical study forward. Our CPMs understand the importance of clear communication & a strong collaboration with the entire project team. Contact us to find out how a CPM can help you succeed in your clinical study. Learn more: https://lnkd.in/diRbSrjg #ClinicalProjectManager #CPM #Careers #clinicaltrials #clinicalresearch #pharma #medicaldevice #clinicalresearchjobs #contractresearchorganization
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Leveraging clinical quality registries for innovative clinical trials Innovation in clinical trials is vital for the future of medical research and development, and clinical quality registries offer significant opportunities by providing a rich source of real-world data. Clinical quality registries collect individual-based clinical data and serve a clinical, scientific and/or public health purpose. In clinical trials, such registries can be used to determine how well randomized controlled trial (RCT) data represent the target population, and provide comparator groups for single-arm trials when RCTs are not feasible or ethical. Further, registries provide an important source of data on rare diseases and patients treated with advanced therapy medicinal products (ATMP), including gene therapy. Clinical quality registries can also be integrated into clinical trial designs to gather data on treatments, outcomes and follow-up. This approach can reduce effort and time commitments for both investigators and study participants. Learn more at: https://lnkd.in/grqS8Mzy #pharma #medicaldevices #genetherapy #biologics #ATMP #clinicaltrials #healthcare #drugdevelopment #clinicaldevelopment #clinicalqualityregistry #dataregistry #patientcare #healthdata #realworldevidence #realworlddata #enablingfuturehealth
Leveraging Clinical Quality Registries for Innovative Clinical Trials | Scandinavian CRO
https://scro.se
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We’re celebrating International Clinical Trials Day this week! Every year on May 20th the world celebrates International Clinical Trials Day, a day that honors the millions of people that have contributed to clinical research over the years. This includes patients, healthcare professionals, regulators, researchers, pharma & medical device professionals, CROs and more. Thank you for your contribution to new treatments & healthcare solutions that improve patients’ lives. Together, we can contribute to better future health for all! Do you need clinical trial support? Visit scro.se to learn more. #InternationalClinicalTrialsDay #ClinicalTrials #ClinicalResearch #healthcare #futureofhealthcare #patientcare #health #pharma #medicaldevices #contractresearchorganization