“We provide high-level expertise in a niche and critical area across the entire clinical supply chain flow, from the planning of the initial drug substance manufacturing to the Investigational Product reconciliation/destruction.”

“By ensuring that pharmaceutical products meet regulatory standards, I contribute to providing patients with access to safe and effective treatments for their medical conditions. This enhances the quality of life for individuals around the world.”

“Statistical consultant services are relevant in many places in the life science industry, we need evidence for everything in Life Sciences.”

“The documents that are produced by medical writing are key to fulfilling regulatory requirements. And they are also keys to successfully advancing a product’s development.”

“In data management, we are technical experts, we develop specific databases to collect and verify patient data according to the protocol approved by the health authorities.”

“A Global Study Manager plays a crucial role in the clinical research industry as we are responsible for the smooth running of the entire clinical study.”

“The Chief Medical Officer plays a key role in ensuring that clinical trials are conducted ethically and on the highest level of patient safety.”

“Our mission is to always be an extension of our sponsor team and not act as a separate entity, a true partnership.”

“Working as a toxicologist in the pharmaceutical industry allows me to contribute to ensuring that patients around the world have access to safe medicines.”

Insights from Matilde Thye Kveiborg, Director of Medical Writing and Tanja Jensen, Senior Medical Writer

Rare diseases are often multifaceted, and a single endpoint is often not sufficient to fully describe treatment

Radiopharmaceutical therapy utilizes radioactive atoms to target and precisely treat cancer cells.