MS Pharm is a service provider established by experienced professionals to provide pharmaceutical companies with the highest level of services. The company is in compliance with all legal requirements, with implemented quality management system and broad experience with audits and inspections. This give us the possibility to be a partner you can rely on.

We are focused on local medical literature monitoring and local pharmacovigilance services across the Europe and CIS countries.

Our strengths are years of experience, our own team of locally based reviewers and professionals, knowledge of local pharmacovigilance requirements.

Our goal is to be the leader in local literature services who will set the standards.

Based on our team of experienced reviewers with medical or pharmaceutical background we cover more than 1.100 non-indexed local medical journals issued in below European countries and CIS countries:

= Bulgaria, Czech Republic, Estonia, Hungary, Latvia, Lithuania, Poland, Romania, Slovak Republic (Central and Eastern Europe)
= Austria, Belgium, Cyprus, Germany, Greece, France, Italy, Liechtenstein, Luxembourg, Malta, Netherlands, Portugal, Spain, Switzerland (Western and Southern Europe)
= Denmark, Finland, Iceland, Norway, Sweden (Nordic countries)
= Albania, Bosnia and Herzegovina, Croatia, Macedonia, Montenegro, Slovenia, Serbia (Adriatic region)
= Armenia, Azerbaijan, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Mongolia, Russian Federation, Tajikistan, Turkmenistan, Ukraine, Uzbekistan (CIS countries)
= Vietnam

MS Pharm in numbers:
>130 MAHs supported
>75 native Reviewers
>50 countries covered
>1.100 journal titles
>300 reports every week
>2.000 substances covered
>8.000 safety reports per year
>5.500 journal issues reviewed per year
>100.000 articles reviewed per year
>3.000 indexed articles containing Safety Relevant Information


Health Care

Life Sciences

Medical Devices

MS Pharm s. r. o.

MS Pharm s. r. o.'s headquarters in Prague 3, Czech Republic

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