Full-service contract research organization (CRO) SynteractHCR will share its Phase I-IV clinical trials expertise as well as its regulatory affairs knowledge at Partnerships in Clinical Trials Europe (PCT Europe), to be held Nov. 17-19 in Hamburg, Germany. The CRO’s global clinical trial experts will be at booth #503 to discuss their services that support the drug development programs of small to mid-sized biopharma companies.
Dr. Martine Dehlinger-Kremer, global vice president of medical and regulatory affairs, will present, “The New EU Clinical Trials Regulation: What Does it Change and What Will the Impact Be to Drug Development in the EU?” on Thursday, Nov. 19th at 11:50 a.m. Her presentation will address the rationale behind changing the previous clinical trials directive as well as the following:
Named one of the 2015 PharmaVOICE 100 Most Inspiring People in Life Sciences, Dr. Dehlinger-Kremer is a leading expert in regulatory affairs. As an advocate for harmonization among regulatory bodies in different countries, she hosted a webinar and has been featured in multiple media outlets on the topic of the New EU Clinical Trials Regulation.
SynteractHCR is a full-service contract research organization with a successful two-decade track record supporting biotechnology, medical device and pharmaceutical companies in all phases of clinical development. SynteractHCR has conducted Phase I-IV studies on six continents and 60 countries, offering expertise across multiple therapeutic areas, with notable depth in oncology, CNS, infectious disease, endocrinology, cardiovascular and respiratory, among other indications. With its “Shared Work – Shared Vision” philosophy and ICD+ approach, SynteractHCR provides customized services collaboratively and cost effectively, ensuring on-time delivery of quality data so clients get to decision points faster.