Medical Affairs
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Medical Affairs
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MEDICAL AFFAIRS
Our team understands the importance of scientific writing and the team prepares very concise and substantive documents. Our medical affairs department comprises of physician, scientific writers and safety experts. We also have a team of practicing physicians as external consultants acting as subject matter experts to provide inputs on major documents like protocol, safety management plan and recruitment strategies.
We follow the practice of integrated review and our medical writing team is fully integrated with the clinical operations, data management and biostatistics departments, to address the function specific requirement. Our team proficiently handles the medical writing activities of drugs, biologics, and medical devices across all clinical phases. All of our deliverables undergo a rigorous quality assurance review to ensure accurate representation and compliance with regulatory requirement.
We specialize in managing the following medical writing services from preparation phase to post marketing phase:
- Preparation of Informed Consent Forms, Dairy Cards and Study Assessment Questionnaires
- Preparation of Medical Monitoring Plan, Safety Management Plan, Study Specific Medical Monitoring and Safety Reporting Processes.
- Preparation of Clinical Study Protocol and Investigator Brochure
- Preparation of Study Procedure Manuals, Study Updates and Newsletters
- Preparation of Abstracts, Manuscripts , Case Studies and Periodic Safety Update Reports (PSUR)
- Collection and Analysis of Key Opinion Leader’s Inputs for Study Design
- Preparation of Clinical Study Reports
- Medical Monitoring
- Pharmacovigilance Services
- Publication Services