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Search for "drug"

Displaying results 1 to 10 out of 18

  Trainings / Workshops 81%
  Trainings / Workshops Workshop In cooperation with iCardiac, CRS is happy to invite you to the upcoming Early Drug Development Workshop: An Alternative to the Thorough QT Trial-EPQT, An International Perspective Location: CRS Clinical Research Services ...
  Size: 29 K - Created: 04-09-13 - Modified: 20-12-17 11:58
Path: /CRS/Trainings / Workshops

  Consultancy 71%
  ... Our professionals have extensive experience with the European Medicines Agency (EMA) and national European regulators as well as the US Food & Drug Administration (FDA). CRS's services include: Setting up clinical study protocols and clinical development plans both in early and late-stage ...
  Size: 30 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/Consultancy

  Pharmacodynamic Expertise 71%
  Pharmacodynamic Expertise The identification of clinical effective drug candidates in the early clinical trial conduct is the key benefit of ... it is possible to distinguish between effective and ineffective drug therapy, which enables “go/no-go” decisions for the clinical drug development programmes of our clients combined with time and cost ... coherence tomography (Talking Eyes ®) Pharmacology Controlled
  Size: 34 K - Created: 18-11-12 - Modified: 02-05-18 10:39
Path: /Expertise/Pharmacodynamic Expertise

  Trial Expertise 71%
  ... have carried out up to 61 studies with respiratory drugs in the past eight years, in healthy volunteers as ... rating in all cases: ‘No Action Indicated’. Food-drug interaction Although in most trials a standard ... specialising in detailed analyses of meals. Drug-drug interaction CRS has performed more than 40 DDI ... More than 22 trials have been published since 1981.
  Size: 34 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Expertise/Trial Expertise

  CTSM & GMP 70%
  ... after receipt, storage, manufacturing steps, QP release, dispensation for administration, drug accountability and return / destruction) according to the regulatory requirements.   CRS ... are located in close vicinity of the clinical sites. This enables preparation and immediate drug administration especially of
  Size: 33 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/CTSM & GMP

  CDM & STAT 68%
  ... Data Management The highly qualified and motivated team has more than three decades of experience in services related to submitting clients’ drugs for regulatory approval and delivering continuously high-quality data. Thanks to its flexibility and experience, CRS can work to clients’ ... separately. Able to handle large quantities of data efficiently, CRS’s highly-qualified team supports data expertise in every phase of
  Size: 31 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/CDM & STAT

  Info-Point 67%
  ... Flyer Your Preferred Partner In Europe For Clinical Trials In Hepatic Impaired Patients Flyer Aging Population - A Challenge In Drug Development Today Flyer Thorough QT/TQT Study – in the Hands of Professionals   Flyer Your Medical Device - Clinical Investigation Is Our ...
  Size: 38 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Info-Point

  2010-2018 66%
  ... in Healthy Male Volunteers Clinical Pharmacology in Drug Development 2018, 00(0) 1–13 2018, The American ... Study Investigating Safety and Pharmacokinetics. Clin Drug Investig. 2018 May 30. doi: ... of letermovir, a novel anti-human cytomegalovirus drug, in patients with renal impairment. Br J Clin ... of Afatinib: An Open-Label, Single-Dose Study. Eur J
  Size: 66 K - Created: 09-11-15 - Modified: 17-07-18 09:33
Path: /Expertise/Published Expertise/2010-2018

  In a Nutshell 64%
  ... and 'large pool of volunteers and patients'. Please feel free to contact CRS directly. Special Fields of Expertise Interaction trials (food, drug & genotype) Thorough QT / QTc Renal & hepatic impairment Respiratory / inhalative devices Women's health / gynaecological examinations Men's ...
  Size: 31 K - Created: 12-08-15 - Modified: 20-12-17 11:58
Path: /CRS/In a Nutshell

  Medical Writing 63%
  Medical Writing A whole range of regulatory and non-regulatory documents is required during clinical trials. The success of drug approval hinges on the quality of these documents – and this is where the Medical Writing Team of CRS comes in. The Medical Writing Team ...
  Size: 31 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/Medical Writing