Pharmacovigilance Safety & Medical Writing
Safety & Medical Writing
Our focus is on TEAM which is why we work closely with you to offer pragmatic solutions and advice on your medical writing requirement to ensure new medicines for patients benefit.
Involving PDS as early as possible helps ensure you as our client has all the information needed to proceed with your development plans. Working with PDS early in the process means we can reduce time and cost, ensuring the project is efficient and successful. Let us provide you with the perfect synergy between theoretical understanding and realtime practical applications.
How can PDS help you
- Investigational Medicinal Products Dossiers
- Investigator Brochures
- Protocols
- Clinical Study Reports (including abbreviated CSRs)
- ICSR narratives
- Informed Consent Forms
- Risk Management Plans
- DSURs
- Clinical Evaluation Reports
- SOP Preparation
- Training Modules
- Medical Information Responses (drafting scientifically accurate and patient-friendly responses to medical information enquiries)
“Knowing is not enough; we must apply. Being willing is not enough; we must do.”
Leonardo Da Vinci
Email us now to discuss your project with one of our Team
Together, we’ll safeguard patient health and maintain compliance with confidence.
