Clinical Phase II-IV Trials - Design, Performance and Evaluation

A key factor of successfully carrying out reliable studies is consistency. This not only applies to uncompromising adherence to predefined study protocols, but to the coherence of the team conducting them. The staff at Inamed is a highly stable unit of professionals, the core of which has been working together for over two decades. Clients benefit directly from this highly effective synergy with studies completed on time, within budget and strictly according to relevant guidelines. The Inamed team represents the cream of the crop – with very little rotation.

Why so many have come aCROss

Coupled by innovative industry firsts, Inamed’s long list of unique Continental European services and worldwide exclusives make it the partner of choice for numerous key decision makers. Just as important as its impressive trial capabilities though, is the reliable structure upon which Inamed’s clinical operations are based. With over two decades of clinical research experience, our clients benefit from streamlined operations designed to provide reliable results, on time and within budget. It’s the ideal combination of scientific expertise and administrative competence. Talk to us and you’ll soon understand why so many companies have already come across.

  • Consulting
  • Protocol Writing
  • Informed Consent Form
  • Preparation of Study documents (such as Case Report Forms, Diaries)
  • Regulatory Affairs / Clinical trial authorization
  • Recruitment of patients or study sites
  • Project Management
  • Monitoring
  • Data Management
  • Biometrics
  • Medical Writing 
  • Presentations at seminars and congresses
  • Preparation of Publications

Inamed's Operational Regions

Operate globally, act locally.

In an increasingly competitive global marketplace, the ability to operate profitably in diverse geographic markets, and to shift operations flexibly between countries may be essential to the success of your business. Understanding and adhering to local laws, regulations and other requirements is vital for the performance of any clinical trial.
Operating globally generates a wide variety of practical, medical, regulatory, legal and finance issues. Multinational projects must comply with host countries' laws and local practices.

We can help. With more than 20 years of experience in performing clinical trials and offices in 32 countries* (presence in 44 countries), INAMED offers the complete range of services for the performance of clinical trials through out all phases, wherever you may need them.

It's all part of our commitment to help you performing your clinical trial challenges locally and around the world.

 

* through strategic Alliances