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They are a full-service global Contract Research Organization (CRO) with over 200 employees in 11 offices across Northern America and Europe offering superior clinical development services to biotechnology, pharmaceutical companies and independent institutions acting as sponsors who wish to have a dedicated and cost effective partner.

psn‘s focus, since inception in 1997, is to provide a personalized alternative to large CROs by offering the highest professional added value.

psn is large enough to cover any kind of clinical development program, but small enough to give the personal attention and flexibility to each project.

Their experts have worked in clinical trials for over 25 years gaining extensive experience in oncology, neurology, cardiovascular diseases, gastroenterology, immunology as well as a host of other therapeutic areas.

psn has developed a competitive cost operational approach based upon a flat management structure with low overheads combined with the highest level of performance and quality standards in clinical development activities.

An unrivalled local expertise on regulatory authority strategies, ethics review processes and relations with specialized investigators enable us to provide proven competitive timelines and exceed Sponsor´s expectations.


Pharmaceutical Service Network LLC
US Head Office
2421 Ivy Rd Suite 200
Tel: +1 434 220 9380
Fax: +1 434 220 9399
EIN Number 27-3763578

EU Head Office
Calle Rufino González 14
Esc. 1ª-2ºD
28037 Madrid
Tel: +34 91 375 69 30
Fax: +34 91 375 69 31


Clinical Trial Supply

psn is experienced in the handling of clinical trials supplies in all countries covered. In particular, psn has developed a special department which holds a good manufacturing practice (GMP) authorisation issued by the Danish Medicines Agency for import, stock, randomisation, labelling, repackaging and distribution of clinical trials supplies. Its clinical trial supply department has developed a…

Data Management & Biostatistics

psn 's main goal is to deliver quality databases on time and within budget. We understand that data analysis is a critical component to each study and its procedures and systems are compliant with ICH and GCP Guidelines, including FDA 21 CFR Part 11.psn offers the following Data Management services adapted to sponsor's requirements:CRF design,…

Medical Affairs

psn provides a professional consulting service by senior executive experts from the pharma and biotech industries. For many years, psn has maintained agreements with a comprehensive panel of well-recognized experts that work cross-functionally on several disciplines and therapeutic areas:Drug development programsMedical assessments and informationEvaluation of in-licensing and acquisition opportunitiesClinical development assessments and plansPre-clinical development assessments…

Monitoring Clinical Trials & Non Interventional Studies

psn offers a unique alternative for starting up and conducting clinical trials and Non Interventional Studies. Local monitors are coordinated by a single study manager located in your country, fully dedicated to your project, producing high-performance results in accordance with local regulations and ICH requirements.Performance is ensured by their personal knowledge of the local Investigators,…


Quality Assurance (QA) and Quality Control (QC) systems and procedures must be implemented by every pharmaceutical company to ensure that the ICH GCP guidelines and applicable regulatory requirements are adhered to during all the stages of a study.psn has significant experience auditing vendors, partners and clients. psn 's QA personnel can assist sponsors and investigators…

Regulatory Affairs

psn offers a wide range of services in connection with registration of human and veterinary pharmaceuticals, medical devices and biotech products from a full registration package or customized deliverable to translation of a simple text into local languages.Local presence and experience give psn a clear advantage in assisting its clients with their regulatory needs. Submission…
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