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"Without standards, there can be no improvement" (Taiichi Ohno)Read more
SynCRO provides consultancy for clinical research sites in the development of QMS and site-specific clinical research SOPs.
In addition, we can perform GCP investigational site audits and vendor qualification audits anywhere in the world.
During the last years there were considerable delays in clinical study approval times in Romania which led to a decreased interest to conduct clinical trials in our country. Towards the end of 2018 the Romanian RA have realized that very prompt and urgent measures must be taken in order to normalize the situation.Read more