Global Infrastructure for Faster Medical Writing Solutions

Whether you're seeking a dedicated team of writers and reviewers to seamlessly integrate with your in-house staff or require assistance in specialised areas, finding a reliable partner is essential. You need someone who can deliver tailored medical writing solutions to meet your unique requirements.

Our team of medical writers offer extensive expertise in medical writing through a freelance/contract basis or via our Functional Service Partnership (FSP) model. We specialise in helping biopharmaceutical, biotech, and medical device companies translate intricate scientific data into clear and compliant statements.

With a solid reputation forged over decades of experience, we provide the necessary talent and knowledge to ensure our clients meet their deadlines. Our approach offers the flexibility, reliability, and continuity required for success in the fast-paced world of medical writing.

By harnessing dependable, top-notch medical writing services that tap into a wide range of therapeutic areas and document knowledge, our solutions offer the ease of collaborating with one global partner for all your medical writing requirements. Our experts offer the adaptability to swiftly adjust based on program and regulatory demands, assisting in all aspects of medical writing throughout the development journey. This encompasses the following key areas:

Preclinical

• Investigational New Drug (IND) modules

• Investigator's Brochures (IB)

• Annual Reports

• Briefing packages

Phase I-III

• Protocols

• Informed Consent Forms (ICFs)

• IB updates

• Clinical Study Reports (CSRs) and narratives

• White papers

Marketing Authorisation Applications

• New Drug Applications (NDA)

• Biologics License Applications (BLA)

Our experienced medical writers have diverse therapeutic backgrounds (including vaccines, rare diseases, neuroscience, oncology etc.), and are adept problem-solvers, consistently delivering documents that meet stringent standards for scientific accuracy and regulatory compliance. Each project is tailored to your specific needs, whether addressing niche service gaps or assembling a robust team of writers and editors. We allocate dedicated resources that align with your organisational culture and values, swiftly adapting resource levels as required.

For solid protocol designs, our medical writers can work with your clinical expert, or alternatively tap into our vast pool of Clinical Scientists or clinical experts/consultants for a tailored solution specific to your study.

Our worldwide network ensures tailored support for clients across different regions and countries, maintaining consistent quality standards globally. With experts situated in diverse locations covering all time zones, our established method fosters successful team dynamics, facilitates knowledge exchange, and fosters productive interactions throughout our collaboration.

Email info@freelanceclinical.com to learn more about how our medical writers help translate complex scientific data into clear and compliant scientific statements so you can meet your timelines.