What We Do
Creation, editing and proofreading of clinical trial documents, including, Protocols, Investigators’ Brochures (IBs), Standard Operating Procedures (SOPs), Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Manuscripts, Brochures, Newsletters, Patient information materials and many more…
Regulatory Support with Submissions
Our team of experts have a wealth of knowledge and experience in regulatory affairs.
We can provide support in the creation of regulatory documents and also assist with the regulatory and ethics submissions in a global capacity.
1:1 Consultancy Support
We can arrange a call to discuss your company or individual needs.
In addition, if you need some ad-hoc advice or regular support, we can provide an expert to assist you.
Our sister company Training Online 4U can provide bespoke training for your company, as well as access to a wide range of interactive and engaging e-learning modules. They can also provide visual training presentations or brochures that can be adapted to your own company’s style.
Ensure Compliance to Regulations and Standards
Regulations and standards are being constantly updated, our team of experts keep up to date to help companies be reassured they are following all the correct guidance.