Medical Writing

Drafting clear, concise and accurate scientific documents requires technical training and enough regulatory and scientific knowledge to ensure that these documents are accepted by Health Authorities as well as by main journals and cutting-edge media in biomedical environment. In addition, previous knowledge of legal regulations and the specific therapeutic areas  (Final Results Report, Abstracts, Posters for conferences, Protocols, Patient Information and Informed Consent Forms, etc.) is required.

Having participated in a large number of clinical studies of different pathologies (oncology, hematology, endocrinology, gynecology, cardiovascular, neurology, etc.) and a large number of clients from different fields (pharmaceutical and medical device industry , independent researchers and biotechnology companies), Experior has the experience required to draft those scientific texts and documents, including but not limited to Protocols, Patient Information and Informed Consent Forms, and Clinical Study Reports (CSR). All the reports related to the dissemination of results generated by Experior are made following the ICH guidelines (ICH E3 Structure and Content of Clinical Study Reports) to ensure that they meet the internationally recognized standards.

Experior offers a customized medical writing service within very tight deadlines. In addition, we are familiar with different writing styles due to our wide  range of clients.

Medical Writing expressed in figures

Protocols developed

Patient Information and Informed Consent Forms drafted

Final
Reports drafted

Methodology

  • We perform the necessary literature searches that support and justify the document.
  • Through personalized meetings according to the needs of our client, we help to design the research studies and establish the steps to be followed.
  • For technical documents we focus on national (AEMPS, ICH E6R2. E3) and international (GDPR) guidelines
  • We contact conference  or scientific journal representatives s to find out the specific standards, conditions and deadlines for publication and facilitate dissemination to clients.
  • A contact person  in the multidisciplinary team is assigned to facilitate contact between the client and Experior.

Other services

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Translation
eCRF
Pharmacovigilance

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Experior continues evolving!

We completed the integration process in the NEUCA Capital Group.
From this moment…

• Experior CRO becomes Clinscience
• Experior SMO becomes Pratia

We grow and consolidate without losing our essence.
We put at your service a new agile structure, a global coverage, an organizational
network and a parent company that gives us stability and strength to meet the
needs of commercial and non-commercial studies.

Welcome to a new era!

Because "the best way to predict the future is to build it," and that is where we are.