A Tried & True Clinical Research Choice

Your trials are supported by 20 years of the on-the-ground experience.

  • Staffed office in Warsaw since 1995
  • Over 20 years of experience conducting trials in the country


Poland Map
Strategic Location with Streamlined Processes

Strategic Location with Streamlined Processes

So you benefit from a regulatory environment that is standardized & predictable.

  • East-Central European country with population of 40 million
  • Legal and administrative framework of EU Directive on Clinical Trials was enacted in 2004
  • Easy and quick transfer of study supplies
Poland Patient

Predictable Patient Profile, but in Greater Numbers

Similar traits ensue, but many more patients able & willing to participate.

  • Greater motivation for Polish patients to enroll vs. mature Western European markets
  • Access to national health system is limited & medications are expensive
  • Free drugs, diagnostic testing & procedures are harder to access, especially when stage of the disease matters with oncology & transplant treatments among the top motivators


Less Trials Overall Means More Opportunity for You

Less Trials Overall Means More Opportunity for You

Get your treatments to market in a viable but underused market.

  • Between 2013 and 2014, trials decreased approximated 10% due to competition from new emerging markets, including Asia
  • Poland boasts high, rapid recruitment rates in nearly all therapeutic indications
  • Data used for the Successful FDA/EMA approval in: ABSSSi (2 IMP), Angina, Asthma, Cervical Dystonia, Crohn's Disease, Hospital Acquired Pneumonia, Migraine, Post-Surgical Pain, Premature Ejaculation, Pulmonary Hypertension, Respiratory Distress Syndrome, Rhinitis (perennial), and Urinary Incontinence

Experienced Staff, Expert Investigators

Experienced Staff, Expert Investigators

Benefit from an active, but not saturated, Latin American trial market.

  • Investigator network is highly experienced, maximizing efficiency and ensuring compliance
  • Full-time Regulatory Specialist (Director, Regulatory Affairs) on site is a PhD, MD, & Pediatrician and has been with Pharm-Olam since 1995
  • On-site Director of Project Management is an MD with 17 years of clinical experience and with Pharm-Olam since 2001
  • Staff includes ENT, Pediatricians, Neurologist, Urologist, GPs and Pharmacists

See why working with Pharm-Olam in Poland could be the best choice for your next study.

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