IDDI, Biostatistical and eClinical Services for Clinical Trials

TRIAL DESIGN - RANDOMIZATION - DATA MANAGEMENT - BIOSTATISTICS
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Home > Content > ADDING VALUE TO BIOTECH

ADDING VALUE TO BIOTECH

Services for biotech companies

Your needs are our obsession

You have restricted resource and budget, yet you have to get your compound into the next phase of development as quickly as possible in order to get positive results for extra funding, or to market your compound or technology to the wider drug development community. Sound familiar? You are therefore looking for a full service CRO, a one-stop shop, since you have limited resources in house. However, with a large CRO, you will not find the premium statistical support that your clinical trial deserves, nor will you get the most out of your money for multiple tasks requiring specific skills.

IDDI is an expert CRO that offers a packaged solution of services and technology that will accommodate your needs now an in the future. We also work with dedicated partners to offer all the services you need if you do not have in-house capacity.

You deserve advanced and innovative statistical designs (such as adaptive Bayesian designs) that can be presented and defended before regulatory agencies and will give your study the very best chance of success or early identification of issues
 

 IDDI is uniquely positioned to provide such high value added statistical expertise, combined with our cost-effective eClinical systems that come highly recommended by your industry peers for successful randomization and Electronic Data Capture.
 

 

Our Solutions:

 IDDI gets you from study start-up to database lock in the shortest possible time without compromising the focus of ensuring the highest accuracy and quality of your data at all times. We do not cut corners but we are nimble and flexible enough to know that you can’t afford anything but getting it right the first time. As a result the overall cost of undertaking data management of the study is lower. 
 

We provide:  

  

  TRIAL DESIGN 

 

  The most optimal design for your trial

 

  

  INTERACTIVE WEB RESPONSE SYSTEMS (IWRS) 

 

  Central randomization and treatment allocation for your randomized trials

 

  

  EDC - DATA MANAGEMENT 

 

  User-friendly and cost effective (e)CRF or EDC (integrated with  IWRS)

  On time and on budget data management

 

 

  STATISTICAL ANALYSES 

 

  Best in class statistical analyses

 

  

  MEDICAL WRITING

 

  Professional medical writing and clinical study reporting

IDDI’s core competence is biostatistics, thanks to our founder, Professor Marc Buyse, who holds a Doctorate in Biostatistics from Harvard University. As a result our philosophy tends to be different from companies purely business driven as we are focused on ensuring you have the best possible data.
 

Want a full service?

  • We work with our dedicated partner network and, unlike others, we don’t mark up our prices. So you will get the best out of each supplier, under one contractual agreement and one invoicing process.
  • Our partners provide Program Management including vendor management, Regulatory Affairs, Drug Supply Logistics, Central Lab-Imaging-Reading Centre, PK-PD, Pharmacovigilance, Clinical Operations –feasibility studies, site selection, site recruitment, site management and monitoring - wherever needed throughout  US, Europe and AsiaPac.

 

TAKE NO RISKS :

Rely on IDDI’s loyal, flexible and responsive team of highly skilled professionals in randomization, data management and statistics. International Drug Development Insitute (IDDI) has served biotech companies for over 22 years and will continue to do so with the same enthusiasm, helping you to bring your compound to market in shorter timelines, on budget and according to regulatory requirements. 
IDDI’s main client base (+65%) are biotechnology companies in both Europe and the United States, so we are very much used to working within this fast-paced environment.