The Association of International Contract Research Organizations (AICROS) is delighted to announce the acceptance of Asymchem Clinical as its newest associate partner. Asymchem Clinical, a leading full-service Contract Research Organization (CRO) with a rapidly expanding global presence, joins our consortium of established, regional CROs dedicated...
Coronavirus research: one step closer to decoding the virus Last updated on 11th January 2021 February 2021: Ending Covid Updates 7 months ago, we started sharing the development of clinical studies on COVID-19 and we have been updating it regularly because we though it could be useful for...
Why choose the Czech Republic to conduct your clinical trial? Czech Republic is one of the Central European countries with a population of 10.65 mil. inhabitants. The other Central European countries are Poland, Slovakia and Hungary (possessing together with the Czech Republic a population of more than 64...
Audits and clinical trials The current focus in the clinical research world is moving into technological transformation. The changes associated with this transformation have the impact on many aspects of clinical trial management, such as risk management, remote monitoring, electronic Trial Master File, electronic patient related documents, electronic...
What is a Contract Research Organisation and how will it make your international Clinical Study easier? A Contract Research Organisation (CRO) is a company that provides support to pharmaceutical, biotechnology and medical device industries through the provision of Clinical Study services outsourced on a contract basis. There...
AICROS experience with COVID There will be always patients requiring innovative treatment solutions, which at times may not be able to wait for COVID-19 to subside. For those cases we would like to see clinical research continuing as best as possible at a normal pace, what...
Why choose Israel to conduct your clinical trial In recent years, Israel has morphed into an emerging and preferred destination for clinical trials, offering high-standard research and medical expertise, a diversified population and short, simple regulatory approval pathways, and relatively low administrative costs. Bigrange of geographical regions...
AICROS and EDC systems We are living in a transition period in relation to the data collection for clinical trials. The trend is that paper-based data collection is replaced more and more by Electronic Data Capture (EDC). In this article we will point out the advantages of...
Conducting Clinical Studies in Australia Why choose Australia? Australia is home to some of the world's best researchers and health professionals and boasts a world-class research infrastructure, with a long and successful history of conducting clinical studies. With a one of the fastest regulatory pathways in the...
The new Medical Devices Regulation 2017/745 (MDR) was supposed to take full effect in Europe by mid-2020, being a fundamental revision of existing Medical Device Directive 93/42 EEC (MDD) and Active Implantable Medical Devices Directive 90/385/EEC (AIMD); following the SARS-CoV-2 outbreak in Europe, on April...