Ready for a career move? Have a look at our current job opportunities in Clinical Operations, Data Management, Regulatory or Drug Safety and consider working for a company which recognizes that its employees are the most valuable company asset. ow.ly/7n8s30q3FH6

We offer a comprehensive portfolio of services, including pharmaceutical, biometrics and medical device. Our services can be tailored to meet the individual needs of each client. Contact us today to see how we can help you ow.ly/4nZg30q3FH8

On 3 Sept 2019, the European Network of Paediatric Research at the European Medicines Agency (Enpr-EMA) opened a public consultation on clinical trial preparedness in paediatrics. Read more in our latest Regulatory Newsletter now available on our website! ow.ly/VHLF30pOQ0w

Are you ready for the new EU Medical Device Regulation? CROMSOURCE Regulatory experts can provide strategic consultancy to support you in getting your product approved! Contact us to learn more. ow.ly/X7Ck30pGSAm

Did you know that 1.2 billion people worldwide need glasses to see better? More than 75% of visual impairments can be avoided with the right resources & treatment. We are dedicated to #ophthalmology research and have been for more than 20 years. ow.ly/rZyI30pDSkc

Have you read our white paper on "Clinical Evaluation of Medical Devices: The Increasing Responsibilities of Clinical Evaluators"? ow.ly/6xg030pr7NG

"The EU Clinical Trials Regulation – Preparing for the changes ahead". The way clinical trials are conducted in the European Union will undergo a major change when the Clinical Trials Regulation EU No 536/2014 becomes applicable towards the end of 2020. ow.ly/AWsS30peSeT

September is Pain Awareness Month. It is estimated that a third of the population lives with chronic pain, defined as pain lasting longer than six months. We are dedicated to working with clients in the area of pain management to help improve their lives ow.ly/pJpS30pr7NI

We support World Alzheimer’s Month to help raise awareness and challenge the stigma that surrounds dementia. There are over 100 forms of dementia, the most well-known is Alzheimer’s disease which accounts for nearly 60% of the cases. #WorldAlzMonth ow.ly/7m3c30pr7NK

As a full service CRO, CROMSOURCE can assist our clients in optimizing scientific, clinical and regulatory product development strategies, in addition to executing these clinical plans and assisting with regulatory submissions. ow.ly/8k8S30p2vAp

Do you plan to market your medical device in the EU? Contact our CROMSOURCE medical device experts today to help you navigate through these new, critical regulations. ow.ly/SCeO30p2vAt

Penta ID Innovation and CROMSOURCE, together for improving drug development for paediatric patients. For further information, please have a look at the following link: lnkd.in/dPA9niw

Customers rely exclusively on our staff to manage all biometrics aspects from rapid data entry to final trial reports. Our experience allows us to make recommendation on the most efficient and cost-effective approach for your clinical research trial. ow.ly/lCNW30p2vAC

@CROMSOURCE welcomes a new member of the Talent Acquisition Unit, ROCIO EGEA MOTA. Rocio has over 20 years’ experience in a variety of industries, including Pharmaceutical, IT and Finance, within Human Resources and functional resourcing.

Read our new white paper "Clinical Evaluation of Medical Devices: the Increasing Responsibilities of Clinical Evaluators" and learn more about the changes and key requirements with respect to conducting clinical evaluations. ow.ly/12DB30oUIGh

For more than 20 years, @CROMSOURCE has been privileged to support trials in a wide range of therapeutic areas and in most major indications. Looking for a global, full-service CRO with international phase I-IV, pre- and post-market trials experience? ow.ly/wQAb30oUIGi

Last week we had the pleasure to host Giuseppe Recchia, Co-Founder and CEO at daVinci Digital Therapeutics, at our Verona Headquarters for a lecture on 'Digital Health, Digital Medicine and Digital Therapeutics'. #DTx

FDA Modernizes Clinical Trials with Master Protocols in 2019 The use of clinical trials with Master Protocol design is one example of a modern approach to expedite the development of oncology drugs and biologics. ow.ly/Edoo30oUIGk

Our flexible, creative approach is designed to meet every client's needs. We understand the needs and challenges facing small and medium-sized companies with respect to quality, timelines and costs. Make sure you choose the right CRO to run your trial. ow.ly/dAkX30oUIGm