Since 2011 MDP Group has excellent experience in many different nosology & fields

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Cardiovascular
& Metabolic
Diseases

  • Diabetes Mellitus-Type 2
  • Diabetes Mellitus-Type 2 (Biologic)
  • Diabetic Nephropathy
  • Hypercholesterolemia (Biologic)
  • Obesity (Biologic)
  • Osteoporosis Treatment and Prevention
  • Osteoporosis Treatment and Prevention (Biologic)
  • Stroke Prevention in Atrial Fibrillation
  • Vasomotor Symptoms of Menopause
  • Venous Thromboembolism Prevention
  • Venous Thromboembolism Treatment
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Inflammation &
Immunology

  • Anti-Inflammatory
  • Lupus
  • Lupus (Biologic)
  • Osteoarthritis
  • Psoriasis (Oral)
  • Psoriasis (Topical)
  • Psoriatic Arthritis
  • Rheumatoid Arthritis
  • Rheumatoid Arthritis (Biologic)
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Neuroscience
& Pain

  • Chronic Pain
  • Epilepsy Monotherapy
  • Migraine (Biologic)
  • Peripheral Neuropathic Pain
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Other areas
Of focus

  • Asthma
  • Chronic Obstructive Pulmonary Disease
  • Chronic Renal Failure
  • Dry Eye
  • Gaucher Disease (Biologic)
  • Hepatitis C Virus
  • Migraine
  • Sleep Disorders
  • Vasomotor Symptoms (Biologic)
  • Vaso-occlusive crisis associated with Sickle Cell Disease
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Clinical Trial
phase capabilities

  • Phase 1: FIM/FIH – Molecular
  • Phase 1: FIM/FIH – Biologic
  • Phase 1: Inpatient – Molecular
  • Phase 1: Inpatient – Biologic
  • Phase 1: Outpatient – Molecular
  • Phase 1: Outpatient – Biologic
  • Phase 2 – Molecular
  • Phase 2 – Biologic
  • Phase 3 – Molecular
  • Phase 3 – Biologic
  • Phase 4 – Molecular
  • Phase 4 – Biologic
  • Sleep Clinic
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By Phase

  • Phase 1
  • Phase 2
  • Phase3
  • Phase4

MDP-group has deep knowledge and experience working with Ministry of Healthcare and local Regulatory Authority.

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Our benefits

Cooperation with the Ministry of Healthcare and  FSBI «Scientific Center of Expertise of Medical Products»

Conducting multicenter global Clinical Trials based on the FDA/EMA requirements

Healthy volunteers database

Conducting registrational Clinical Trials

Providing full support

  • GCP standards
  • FDA/EMA standards
  • Patients enrollment with and within our sites in our region (Russia and Eastern Europe)
  • Logistics
  • Full Data management and support with own EDC platform
  • Monitoring and reporting
  • Pharmacovigilance
  • Final integrated reporting
  • Registration
  • Distribution