Whether part of full-service CRO trial management or as a stand-alone service, Advanced Clinical’s medical writing services provide exceptional results from doctorate-trained writers. Our fact sheet offers information on how we deliver:
- Clinical study reports (CSRs)
- Pharmacodynamic reports
- Pharmacokinetic reports
- Protocols
- And more
Our Medical Writing Expertise
Advanced Clinical’s writers bring extensive knowledge and experience to every job, offering an array of benefits, including:
- A team whose members are located across the globe
- Fast, flexible and focused regulatory writing
- More than 12 years of industry experience on average
- An understanding of ICH E3 guidelines
A Documented History
Our experienced team offers extraordinary medical writing because their previous experiences allow them to apply the wisdom gleaned from the past to every task that follows. When you partner with Advanced Clinical for your medical writing, you get a collaborative, transparent partner who aligns your needs with hard-earned knowledge, resulting in compliant communications that relay your key messaging while adhering to timelines.
Our fact sheet offers more detail on how Advanced Clinical’s expert medical writers meet every requirement, through:
- A collaborative approach
We believe in working closely with partners to ensure alignment - Milestone management
We discuss and adhere to pre-defined timelines - Efficient project management
We handle simultaneous project activities and in parallel reviews - Adaptability
In-depth knowledge of guidelines and creative solutions help us meet emergency situations
Feel Secure With Our Medical Writing Services
Gain confidence in the regulatory submission and other communication requirements your clinical trial demands. Advanced Clinical’s experienced medical writers offer a wealth of knowledge centered on global regulations, including a deep understanding of FDA and EMA regulations. Our fact sheet offers more information on how our collaborative medical writing services can help you stay compliant and on schedule.
Learn how our global team can advise you on region-specific requirements for all your regulatory medical writing needs.
