The process for new drug approvals and medical devices relies heavily on the quality of documentation submitted to the regulatory authorities, and a high standard of medical writing plays a vital role in ensuring a positive outcome.
Our medical writing training courses will provide delegates with all the tools and techniques necessary to comply with the required standards.
Our expert team of speakers has extensive knowledge and expertise in this specialist area.
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
How to produce quality regulatory documents including the clinical evaluation report (CER)
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.