Regulatory Writing Services for Clinical Trials

Regulatory Writing Services-Pharma | Biotech | Medical Device Companies

We offer a wide range of high quality regulatory and clinical writing services and also compliant to the regulations that are required to be followed. We ensure that all our writing documents meet your medical, legal and regulatory requirements.
Our regulatory writing is structured in ways that are of the most acceptable norms. Our writing reflects clarity and succinctness, and we adhere to timely delivery of your documents.
Our team of regulatory writers are versatile and experts in the field with more than substantial experience.
We have experience with an extensive range of therapeutic areas including oncology, vaccines, diabetes, endocrinology and neurology. Medical writing Experts present to you a top notch professional writing service in a niche market.
Our regulatory writing services includes
• Phase 1 to 4 clinical study reports (CSRs)
• Protocols and protocol amendments
• Informed Consent and Patient Brochures
• Patient Safety Narratives and patient profiles
• Common Technical Document (CTD) for clinical and non-clinical procedures
• In-House Data Summaries
• Safety Surveillance Plan
• Case Report Forms
We ensure to provide the required assistance to you from day one till the very final completion that ends with your regulatory submission and acceptance. Our writing remains unparalleled so avail our regulatory writing services now!

Contact us:
US/Canada: +1-972-502-9262
UK: +44-1143520021
India: +91-8754446690
Email: [email protected]
Web: http://www.medicalwritingexperts.com/