Call Us:
+1 302-357-9981

Email Us:

Medical Writing

Expert Medical Writing Services for the Healthcare
and Life Sciences Industries

Medical writing is the skillful line of work of creating clear, concise, and accurate documents that effectively convey complex scientific information to diverse audiences within the healthcare and life sciences industries. This specialized form of writing requires a deep understanding of medical language, terminology, and concepts, as well as the ability to distill intricate research findings into engaging and accessible content.

Medical writing skillful use of language to communicate complex scientific information healthcare professionals, researchers, patients, and regulatory authorities. Medical writing professionals must possess a thorough knowledge of regulatory requirements, industry guidelines, and best practices to ensure that documents meet the highest standards of quality, accuracy, and compliance.

Regulatory Compliance and Medical Writing Expertise

At ADI our medical writers are familiar with relevant ICH guidelines, such as those for Clinical Study Protocols and Investigator’s Brochure(ICH E6), Structure and Content of Clinical Study Reports (ICH E3), and Common Technical Document (ICH M4).

Our team of writing professionals is uniquely qualified to assist you in assembling, organizing, writing, editing, and producing medical and scientific documentation to support product development. We deliver:

At ADI Intellect, we specialize in providing comprehensive medical writing services to pharmaceutical, biotechnology, and medical device companies worldwide. Our team of highly skilled medical writers and subject matter experts work together to deliver high-quality documents that meet the diverse needs of our clients.

Our Expert Medical Writing Services

We have a deep understanding of medical language, scientific research, and regulatory requirements, ensuring that our documents are clear, precise, and compliant with industry standards. Our medical writers possess a deep understanding of:

Medical language and terminology

Scientific research and principles

Regulatory norms and guidelines

Our Expertise

Our medical writing professionals are experts in:

Clear, Credible, and Compliant Content 

We ensure that every document we produce reflects the utmost precision and clarity, covering all phases of clinical trial documentation, including:

Our Services

Our medical writing services include:

Good Clinical Practices (GCP)

We adhere to globally accepted ethical and scientific quality standards, known as Good Clinical Practices (GCP), which control the planning, execution, documentation, and reporting of clinical studies involving human participants. Our writers ensure that all documents comply with GCP principles.

Clinical Trial Protocols

Our medical writers specialize in creating detailed clinical trial protocols that serve as blueprints for conducting clinical trials. These documents provide a roadmap for researchers and clinicians involved in the study, outlining critical information such as study objectives, eligibility criteria, and analysis plans.

Regulatory Requirements

We understand the importance of regulatory compliance in the pharmaceutical industry. Our writers are knowledgeable about stringent standards, guidelines, and procedures established by government agencies, such as the FDA and EMA, to ensure the safety, and proper labeling of pharmaceutical products.