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.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
In-house & bespoke training
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Rated by attendees to the public programme
Typically presented by Barbara Grossman (bio)
Typical duration: 1 day | |
Pricing from £450 per attendee | |
Delivery: collaborative classroom |
In-house & bespoke training
How to produce quality regulatory documents including the clinical evaluation report (CER).
Rated by attendees to the public programme
Typically presented by Janette Benaddi (bio) , Barbara Grossman (bio)
Typical duration: 2 days | |
Pricing from £800 per attendee | |
Delivery: collaborative classroom |
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Cheryl Roberts-Vitalis (bio)
Typical duration: 3 days | |
Pricing from £1,200 per attendee | |
Delivery: collaborative classroom |