Medical Writing Services

Have you ever wondered what distinguishes average writing assistance from an excellent medical writing service?

It is not just about having expert Medical Writers in our team (which we do). It is more than having a straightforward communication process with our clients (which we are proud of). It is the peace of mind that you will have knowing that, no matter the type of project, you can trust that all your scientific documentation is in good hands.

Across a wide range of therapeutic areas, LS Academy helps you prepare clear, readable documents, within:

We know, as well as you do, that:

Readable, reviewer-friendly regulatory documents are key to market access
Clear, understandable medical communications materials are essential to stakeholders’ engagement

But too often, the preparation of these important documents is overlooked, creating inaccurate, obscure texts that waste your time and resources. Whether because there is no in-house writing team or there is a deadline looming, sometimes it is hard to keep up with the demand. This has a considerable impact on your pharmaceutical and medical device products, but also on the health of patients that benefit from them.

At LS Academy, we understand how important your scientific documentation is.

With our team of dedicated Medical Writers, we provide high-quality medical writing support across a wide range of therapeutic areas within Pharmaceuticals and Medical Devices, throughout the entire lifecycle of your product, from product and drug development, passing through all submission phases and to post-market surveillance.

We know that different audiences require different types of communication. A data analysis for clinical or nonclinical summaries demands different skills from our medical writers than a patient-centric information sheet regarding enrolment in a phase III clinical trial.

Nevertheless, the solutions provided by our team of experts can accommodate all your different requirements.

Here are some of the documents we can help you prepare:

Research Protocols and amendments
Clinical Investigation Plans
Clinical Study Reports (Phase I through IV)
Common Technical Document (CTD)
Periodic Safety Update Reports
Safety Narratives
Scientific Manuscripts
Website Content
Training Material for Healthcare Professionals
Patient information (including Informed Consent Forms)
Lay Summaries
Clinical Evaluation Reports
Literature Reviews
Technical or Marketing Brochures
Annual reports

Drawing from our expertise and years of experience, we want to help you achieve your goals. Whether it is a new drug submission, a literature search, or a multi-step project, you can be sure that our solutions will surpass your expectations.

Want to know more?

Contact us for a compromise-free call at medicalwriting@lsacademy.com
We would love to help.