London, UK: +44 (0)20 3983 7341 | Cambridge, Massachusetts: 617-674-2650 | San Mateo, California: 650-378-1270
To ensure compliance with evolving global and European regulations in various areas of drug safety, we offer solutions in:
Safety reporting in clinical trials
Risk management and Periodic Reporting
Pharmacovigilance Database: Data Entry, Medical Review and Expedited Reporting
QPPV and pharmacovigilance systems
The scope spreads from ad hoc consultancy on scientific or operational aspects to packaged solutions, crafted to your specific circumstance. Please click here for more information
Regardless how early you are in pre-clinical explorations or late in clinical drug development, we will help you maximise the value of your compound. Our main areas of expertise are:
We can optimise your clinical development program to demonstrate clinical value based on budgetary and time constrains, advise on clinical trial design, and support you throughout your progress.
We believe that it is never too early or too late to make sure that your products are set to maximize return on investment. We specialize in the following areas:
Our marketing plan will leverage clinical data, regional commercial micro- and macroenvironment, competition and regulatory environment to support your strategic targets.
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©2020 Olexacon Limited. All rights reserved.
Registered office: Olexacon Limited, One Kingdom Street,
London, United Kingdom, W2 6BD
Phone: +44 (0)20 3983 7341; email:
info@olexacon.com
Registered in England
and Wales, company number: 9110477. VAT Registration Number: 193
8092 76