We are acting with flexibility, the experience of more than 120 clinical trials and open communication with you in a joint team to ensure your milestones by managing:
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Project
planningCompilation of project management plan and definition of key parameters (milestones, budgets, resources, logistics, project tools)
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Project
performanceBudgeting and cost management of development projects. Resources management and co-ordination of all third party providers contracted
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Quality
assuranceQuality is the backbone of a clinical trial. Our systematic approach ensures high-quality data and is the basis of our daily business.
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Risk
managementA proper risk assessment is used to plan the details of trial management and the approach to and extent of monitoring and controlling the trial
Sacura‘s employees covered key functions in more than 120 clinical trials open third tab
Our Team worked on following international Phase II - IV studies open third tab
- Antiinfective drugs
Quinolones (gyrase inhibitors)
Cephalosporins
Macrolides
Skin and subcutaneous tissue disorders
Onychomycosis
Brittle nail syndrome
Psoriasis
Respiratory disorders
Acute asthma
COPD
Exacerbation of chronic bronchitis
and acute bronchitis (Paediatrics)
Pneumonia
Maxillary sinusitis
Infections
Influenza
H5N1
HIV
Sepsis
Blood and lymphatic system disorders
Tonsillitis
Ear and labyrinth disorders
Otitis media
Acute tinnitus
Endocrine,Metabolic and Nutrition disorders
Diabetes mellitus type I / II
Impaired glucose tolerance
Hypercholesterolemia
Partial androgen deficiency of
aging males (PADAM)
Dyslipidaemia (primary/mixed) -
Frederickson Types IIa & IIb
Low HDLc - Gastrointestinal disorders
Irritable bowel disease
Gastro esophageal reflux
disease (GERD)
Mucositis in children and adults
undergoing stem cell transplantation
Cardio and cardiovascular diseases
Coronary heart disease
Hypertension
Renal and urinary tract diseases
Pyelonephritis
Urinary tract infection
Stress urinary incontinence
Mixed urinary incontinence
Overactive bladder
Renal impairment
Reproductive system and breast disorders
Dysfunctional uterine bleeding
Endometriosis
Benign prostate hyperplasia
Erectile dysfunction
Premature ejaculation
Musculoskeletal and bone diseases
Rheumatoid arthritis
Osteoarthritis of the knee
Postmenopausal osteoporosis
Nerve system disorders
Vascular dementia
Alzheimer's disease
Post herpetic neuralgia
Painful diabetic neuropathia
Restless legs syndrome
Chronic non-malignant pain
Multiple sclerosis
Spinal cord injury - Psychiatric disorders
Schizophrenia
Tumor diseases
Breast cancer
AML
CLL
SCLC
Osteosarcoma
Metastatic epithelial tumor cells
diagnostic in mamma and
colon carcinoma patients
Congenital, familial and genetic disorders
Amyloidosis (Familial amyloid polyneuropathia, FAP)
Hereditary angioedema
Immune system disorders
Neutropenia
Pediatric diseases
Neonatology
Other
Parenteral nutrition
Vitamin C
Radiographic contrast media
Medical devices
Our regions of activity open third tab
- Argentina
Austria
Belgium
Canada - Denmark
Finland
France
Germany - Great Britain
Hungary
Ireland
Israel - Italy
Lithuania
Netherlands
Norway - Portugal
Poland
Spain
Suisse - Sweden
Ukraine
United States
Russia
Long-term and orphan drug experience with specific focus of authorities on control of these studies enables us to implement the current thinking of the FDA and EMA in our daily activities.open fourth tab
- Inspections-related Track Record of our team:
FDA Site and TMF inspection, Germany/USA, April/June 2012
MoH GCP inspection, Argentina, September 2011
Mock inspection, Germany, December 2011
Mock inspection, Germany/USA, May 2011
Mock inspection, Germany, November 2010
FDA inspection, Austria, March 2008


