PharmaPart

PharmaPart is an established, mid-sized, drug development company providing a wide range of services primarily to the pharmaceutical industry and also biotechnology and medical devices companies.

Advantages for your Business

The advantages that PharmaPart can bring to your business are:

• A comprehensive set of services, implemented quickly to ensure your clinical studies, regulatory submissions and data management requirements are fully met and provided on time.
• A very strong planning approach to ensure everything is done to reach your required goal.

Why PharmaPart?

PharmaPart can do this because we have:

• Highly experienced staff - this is the key to being able to plan and implement projects tailored to need your individual needs. Our people are very experienced, flexible and highly competent, In comparison to many CROs, the company has a high percentage of medical doctors and staff with other degrees. Our key professional staff have all worked for many years in big Pharma.
• Proven expertise over many years, in running clinical studies both large and small in Western and Central Europe. These projects have covered a wide range of medical areas including oncology, rheumatology, infectiology, cardiology, psychiatry and dermatology. Additional specific fields in which the company has expertise are herbal medicines and medical devices.
• The ability to quickly put together specialist teams for clinical trials, regulatory affairs, statistics and data management.
• The quality you would expect from an expanding Swiss company founded in 1992.
• Active offices covering Western and Central Europe including the headquarters in Switzerland and offices/representatives in Germany, Romania, Poland, Spain and Portugal.
• A strong financial foundation both independantly and as a member of the Pierrel group of companies. Membership of the group provides access via other members to additional services in the drug development life-cycle including: trial supplies, full production capabilities (CMO) and Phase I services.
• Solid, yet innovative infrastructure and business processes to support your development projects, including: Remote Data Entry (RDE) and electronic Common Technical Documents (eCTD). These capabilities come from being in the CRO business for many years and having often developed many of the innovative approaches now commonly found in the market.

Services offered are based on many years experience in the design, implementation and auditing of projects conducted for a large number of satisfied clients. Examples can be found on the references page.

We welcome your interest in PharmaPart and would like to be considered as a supplier for your drug developments in the future. Feel free to contact us directly from the contacts page, or use the enquiry form or simply send us an e-mail.