Medical Writing for Pharma
Expert Pharma Writing
Regulatory & Scientific Writing for Pharma
We have expertise in the development of various clinical study protocols. Using just the clinical concept, we can help you draft study design, and statistical strategy to ensure valid outcomes. Our team of experienced medical doctors will ensure all the documents are compliant to the highest scientific and ethical standards.
Our services
What We Do for Pharma
We offer services for all stages of development ranging from small start-up firms to global pharmaceutical companies. MediCog’s experienced medical doctors can help get your product to patients faster. All our documents are made in accordance with international guidelines.
Study Protocols
Expertly crafted study designs ensuring compliance with scientific standards.
Case Report Forms (CRFs)
Structured clinical data collection forms to support reporting and analysis.
Study Questionnaires
Tailored data collection tools designed to meet clinical study.
Investigator Brochures
Regulatory documents detailing Investigational product information.
Informed Consent Forms
Compliant documents ensuring ethical patient participation.
Clinical Study Report
Analysis of study data ensuring regulatory compliance and accuracy.
Our Process
How We Work
Our streamlined process ensures the delivery of high-quality results that adhere to all regulatory requirements, industry standards, and client expectations.
Concept to Draft
Regulatory Documentation
Submission & Compliance Support
Scientific Validation
Compliance & Ethical Review
Our Process
How We Work
Our streamlined process ensures the delivery of high-quality results that adhere to all regulatory requirements, industry standards, and client expectations.
Concept to Draft
Scientific Validation
Regulatory Documentation
Compliance & Ethical Review
Submission & Post-Approval Support
What Sets Us Apart
Why Choose Us?
Our team is expert in regulatory documentation including Investigational New Drug Submissions (IND) and Investigational Device Exemptions (IDE).
Expert Medical Doctors
Our team consists of experienced medical doctors who have run clinical studies throughout all stages of product development.
Unparalleled Insights
Our team has worked on drugs and devices phase 1-IV clinical trials providing expert insights.
Strong US presence
We have a strong US workforce and footprint providing you customized solutions.
What Sets Us Apart
Why Choose Us?
Our team is expert in regulatory documentation including Investigational New Drug Submissions (IND) and Investigational Device Exemptions (IDE).
Expert Medical Doctors
Our team consists of experienced medical doctors who have run clinical studies throughout all stages of product development.
Unparalleled Insights
Our team has worked on drugs and devices phase 1-IV clinical trials providing expert insights.
Strong US Presence
We have a strong US workforce and footprint providing you customized solutions.