Accelerate Your Clinical Research with 3SPharma

With 25+ years of experience, FDA & EMA approvals, and fast-track regulatory pathways, we streamline clinical trials from Phase I to IV.

More than 25 years of
Clinical research experience

Headquarters

  • Harpstedt – Germany

Bio-analytical Services

  • Bucharest – Romania

Clinical Research Centers

  • Dedicated Clinical research unit in Romania
  • Phase I-IV Units in Romania & Moldavia
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Key

Benefits

2 fda positive outcome

Recently inspected by FDA & EMA with positive outcome

fast track approval

Fast-track approvals – regulatory clearance in just 2 weeks

clinical studies conducted worldwide

Over 1,500 clinical studies conducted worldwide

1 clinical research facilities

Dedicated clinical research facilities in Romania & Moldova

early phase trials biosimilars and special populations

Expertise in early-phase trials, BA/BE studies, biosimilars, and special populations

Our Expertise

Early Development Studies – First in Human

Early Development Studies – First in Human, PK studies

Transdermal Research Topical Corticosteroid Evaluations

Transdermal Research & Topical Corticosteroid Evaluations

Bioavailability Bioequivalence

Bioavailability / Bioequivalence (BA/BE) Studies

Irritation Sensitization Adhesion Performance Studies

Irritation, Sensitization & Adhesion Performance Studies

Drug Interaction Special Population Trials

Drug Interaction & Special Population Trials

Social Proof &
Compliance

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