Clinical Trials and Development Services

CEPHA'S Headquarters are located in Pilsen, Czech Republic
CEPHA's Headquarters are located in Pilsen, Czech Republic.
Phase 1 Clinic accommodates up to 40 volunteers
The subjects are under full medical control at Phase I Clinic.
High throughput in biological samples processing is a key to effective drug analysis
Timing of blood sample collection is critical step in pharmacokinetic studies.
The bioanalytical lab provides time-effective new HPLC methods development and validation
High throughput in biological samples processing is a key to effective drug analysis.
The state-of-the-art HPLC equipment with tandem mass spectrometer
The latest analytical technology is applied for the determination of trace drug levels in complex matrices.

Integrated procurement services for pharmaceutical products
Komtur Pharmaceuticals is a leading provider of integrated procurement services for pharmaceutical products.
Clinical trials procurement services
We offer international procurement services for clinical trials.
Downstream clinical distribution
Komtur offers a downstream clinical distribution service.
Clinical distribution of reference and study drugs
We can carry out the clinical distribution of reference and study drugs.
International drug distribution services
We support manufacturers with a range of international drug distribution services.


We’re changing the way technology is used in clinical trials. Contact us today to find out how you can benefit.

Plug into our new integrated eClinical Suite.

Can your EDC system dispense medication? Ours can.


SydPath's Central Laboratory Service was established in 1995, and has quickly established its reputation as a top class provider of central laboratory services within Australia.

SydPath participates in both pharmaceutical- sponsored drug trials and grant-funded research as a local laboratory site for its St. Vincent's campus based researchers, as well as for locally based GPs.

We will tailor our services to meet your specific needs, which may include the provision of pathology collection kits, investigator manuals and transport materials.


The fifth annual Pharmacovigilance and Risk Management conference will be held 1-2 December 2009 in Brussels, Belgium.

The conference will provide an opportunity for pharma and biotech professionals to come together to discuss how to develop a robust pharmacovigilance strategy in which there are no gaps.

The conference is tailored to maximise the sharing of knowledge and expertise surrounding the important issues of pharmacovigilance and risk management.


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