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Search for "subject"

Displaying results 1 to 10 out of 15

  Early Phase I to IIa 81%
  ... large trials (mono- or multi-centric) Decentralised subject recruitment Central modular services for all ... studies and the long-term nutrition of hospitalised subjects) can be easily met without affecting laboratory ... volunteers and patients to ensure wide variety of subjects for its clients. CRS currently has more than 28,000 ... including allergic, hypertensive and hyperlipidemic
  Size: 32 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/Early Phase I to IIa

  News 4 80%
  ... safety profile according to the SMPC Clinical conduct in 6 months with more than 100 healthy subjects IMP preparation & labelling immediately prior to dosing under GMP conditions Integration of ... of two clinical sites of CRS to enable simultaneous dosing in small subgroups of max. 4 subjects per day and site Strict standardisation of the working procedures and copperation with two ... several hours Results: Clinical duration in strict adherence to the timeline commitment, the
  Size: 31 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Home/News 4

  Special Populations 78%
  ... updated. For one successful clinical trial, elderly subjects had to be recruited who were more than 75 years old ... the recruitment of a substantial number of elderly subjects. Post-menopausal women: In recent years, studies ... is part of CRS’s standard routine. Genotyped Subjects: Over 3,000 healthy
  Size: 33 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Expertise/Special Populations

  Trial Expertise 75%
  ... data for dose escalation meetings one week after last subject dosed in a particular dose group. Safety and ... on the molecule. Cardiac safety trials in healthy subjects and patients About 3–5 trials annually are cardiac ... as well as in patients with COPD/asthma (ca. 1700 subjects). In this field, CRS has successfully accomplished ... drugs, CRS has access to a broad range of genotyped
  Size: 35 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Expertise/Trial Expertise

  Expertise 75%
  ... more than three decades, CRS has developed particular expertise in the recruitment of challenging populations in terms of sample size (> 200 subjects) and specification (patients, postmenopausal women, senior citizens, etc.) as well as the implementation of challenging trial designs ...
  Size: 30 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Expertise

  Mannheim 71%
  ... In one of its trials in 2009, CRS-Mannheim accomplished an outpatient trial with up to 200 subjects per day over several weeks. Three large laboratories are equipped for infusion studies and ... designs. This unit is dedicated to conducting large-scale trials such as QTc (more than 200 subjects) and long-term trials (overnight stays up to 56 days). Additionally, the unit has special ... University Hospital owing to clients’ growing need for clinical trials with large groups of
  Size: 33 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Locations/Mannheim

  Mailing Campaign (Kopie Home) 71%
  ... units with over 275 beds in Germany High quality - multiple authority inspections (FDA, EMA, BfArM, AFSSAPS, ANVISA, DHMA, etc.) Broad panel of subjects - access to patients, special populations and healthy volunteers      EcoVadis - CSR Rating Based on the CSR rating by EcoVadis in July ...
  Size: 33 K - Created: 11-01-17 - Modified: 20-12-17 11:58
Path: /Home/Mailing Campaign (Kopie Home)

  Locations 70%
  ... Accessibility to several million people is one of the basics for effective recruitment of patients, healthy volunteers or symptom bearing subjects, a prerequisite for the conduct of large scale, long-standing clinical trials and early proof of concept. Locations & Special Fields of ...
  Size: 33 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Locations

  2010-2017 69%
  ... supportive care antiemetic, on the ECG of healthy subjects: an ICH E14 thorough QT trial. Springerplus. 2014 ... A , Koenen R. . Pharmacokinetics of afatinib in subjects with mild or moderate hepatic impairment. Cancer ... H. Pharmacokinetics and safety of teneligliptin in subjects with hepatic impairment. Clin Pharmacol Drug Dev. ... of a dry powder ciprofloxacin formulation in healthy
  Size: 65 K - Created: 09-11-15 - Modified: 20-12-17 11:58
Path: /Expertise/Published Expertise/2010-2017

  Mönchengladbach 64%
  ... pharmacology trials in all standard designs. CRS-Mönchengladbach is dedicated to implementing large-scale trials such as QTc (more than 150 subjects) and long-term trials (overnight stays up to 46 days) combined with challenging PK and PD schedules. In addition, the unit has special ...
  Size: 32 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Locations/Mönchengladbach

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